APP - amyloid beta precursor protein Gene

Also Known as AAA; AD1; PN2; ABPP; APPI; CVAP; ABETA; PN-II; preA4; CTFgamma; alpha-sAPP

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 351

About APP

Cytogenetic location: 21q21.3 Genomic coordinates (GRCh38): 21:25,880,550-26,171,128 (from NCBI)

This gene has 17 transcripts (splice variants), 280 orthologues, 2 paralogues and is associated with 9 phenotypes. Ubiquitous expression in brain (RPKM 395.2), kidney (RPKM 282.2) and 25 other tissues.

Summary

This gene encodes a cell surface receptor and transmembrane precursor protein that is cleaved by secretases to form a number of peptides. Some of these peptides are secreted and can bind to the acetyltransferase complex APBB1/TIP60 to promote transcriptional activation, while Others form the protein basis of the amyloid plaques found in the brains of patients with Alzheimer disease. In addition, two of the peptides are antimicrobial peptides, having been shown to have bacteriocidal and Antifungal activities. Mutations in this gene have been implicated in autosomal dominant Alzheimer disease and cerebroarterial amyloidosis (cerebral amyloid angiopathy). Multiple transcript variants encoding several different isoforms have been found for this gene. [provided by RefSeq, Aug 2014]

APP Products (11)

mRNA Protein Name
NM_001136130.3 NP_001129602.1 amyloid-beta precursor protein isoform f precursor
NM_001204303.2 NP_001191232.1 amyloid-beta precursor protein isoform j precursor
NM_201413.3 NP_958816.1 amyloid-beta precursor protein isoform b precursor
NM_001136131.3 NP_001129603.1 amyloid-beta precursor protein isoform g
NM_001204301.2 NP_001191230.1 amyloid-beta precursor protein isoform h precursor
NM_000484.4 NP_000475.1 amyloid-beta precursor protein isoform a precursor
NM_001136016.3 NP_001129488.1 amyloid-beta precursor protein isoform d
NM_001204302.2 NP_001191231.1 amyloid-beta precursor protein isoform i precursor
NM_001385253.1 NP_001372182.1 amyloid-beta precursor protein isoform k precursor
NM_001136129.3 NP_001129601.1 amyloid-beta precursor protein isoform e precursor
NM_201414.3 NP_958817.1 amyloid-beta precursor protein isoform c precursor
Molecular Function GO Annotation Evidence Références Source
enables G protein-coupled receptor binding IPI
IPI: Inferred from physical interaction
11316806 GOA
enables PTB domain binding IPI
IPI: Inferred from physical interaction
12805363 GOA
enables RAGE receptor binding IPI
IPI: Inferred from physical interaction
22406537 GOA
enables acetylcholine receptor binding IPI
IPI: Inferred from physical interaction
10681545 GOA
enables apolipoprotein binding IPI
IPI: Inferred from physical interaction
9211985 GOA
enables chemoattractant activity IGI
IGI: Inferred from genetic interaction
11316806 GOA
enables chromatin binding IGI
IGI: Inferred from genetic interaction
19057576 GOA
enables enzyme binding IPI
IPI: Inferred from physical interaction
17112471 GOA
enables ephrin receptor binding IPI
IPI: Inferred from physical interaction
21113149 GOA
enables frizzled binding IPI
IPI: Inferred from physical interaction
18234671 GOA
enables heparan sulfate proteoglycan binding IMP
IMP: Inferred from mutant phenotype
21289173 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
16193067 GOA
enables insulin receptor binding IPI
IPI: Inferred from physical interaction
19406747 GOA
enables integrin binding IDA
IDA: Inferred from direct assay
21126803 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
2119582 GOA
enables protein heterodimerization activity IPI
IPI: Inferred from physical interaction
18568035 GOA
enables protein homodimerization activity IPI
IPI: Inferred from physical interaction
15447668 GOA
enables protein serine/threonine kinase binding IPI
IPI: Inferred from physical interaction
24305806 GOA
enables protein-folding chaperone binding IPI
IPI: Inferred from physical interaction
9228033 GOA
enables receptor ligand activity IDA
IDA: Inferred from direct assay
29518356 GOA
enables serine-type endopeptidase inhibitor activity IDA
IDA: Inferred from direct assay
10652580 GOA
enables signaling receptor activator activity IDA
IDA: Inferred from direct assay
11316806 GOA
enables signaling receptor binding IPI
IPI: Inferred from physical interaction
19849849 GOA
Biological Process GO Annotation Evidence Références Source
involved in G protein-coupled receptor signaling pathway IDA
IDA: Inferred from direct assay
11160457 GOA
involved in G protein-coupled receptor signaling pathway IGI
IGI: Inferred from genetic interaction
11160457 GOA
involved in adenylate cyclase-activating G protein-coupled receptor signaling pathway IGI
IGI: Inferred from genetic interaction
22500019 GOA
involved in adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway IDA
IDA: Inferred from direct assay
18723082 GOA
involved in adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway IGI
IGI: Inferred from genetic interaction
20141570 GOA
involved in amyloid fibril formation EXP
EXP: Inferred from Experiment
9737846 GOA
involved in amyloid fibril formation IMP
IMP: Inferred from mutant phenotype
25620700 GOA
involved in antibacterial humoral response IDA
IDA: Inferred from direct assay
20209079 GOA
involved in antifungal humoral response IMP
IMP: Inferred from mutant phenotype
20209079 GOA
involved in antimicrobial humoral immune response mediated by antimicrobial peptide IMP
IMP: Inferred from mutant phenotype
20209079 GOA
involved in associative learning IGI
IGI: Inferred from genetic interaction
19118188 GOA
involved in astrocyte activation IDA
IDA: Inferred from direct assay
18723082 GOA
involved in astrocyte activation IGI
IGI: Inferred from genetic interaction
15457210 GOA
involved in astrocyte activation involved in immune response IGI
IGI: Inferred from genetic interaction
23152628 GOA
involved in calcium-mediated signaling IDA
IDA: Inferred from direct assay
11160457 GOA
involved in calcium-mediated signaling IGI
IGI: Inferred from genetic interaction
11160457 GOA
involved in cellular response to amyloid-beta IDA
IDA: Inferred from direct assay
29518356 GOA
involved in cellular response to amyloid-beta IGI
IGI: Inferred from genetic interaction
23152628 GOA
NOT involved in chemical synaptic transmission IDA
IDA: Inferred from direct assay
18216187 GOA
involved in defense response to Gram-negative bacterium IDA
IDA: Inferred from direct assay
20209079 GOA
involved in defense response to Gram-positive bacterium IDA
IDA: Inferred from direct assay
20209079 GOA
involved in innate immune response IMP
IMP: Inferred from mutant phenotype
20209079 GOA
involved in learning IMP
IMP: Inferred from mutant phenotype
11140684 GOA
involved in learning or memory IGI
IGI: Inferred from genetic interaction
15457210 GOA
involved in learning or memory IMP
IMP: Inferred from mutant phenotype
11880515 GOA
involved in low-density lipoprotein particle mediated signaling IDA
IDA: Inferred from direct assay
26005850 GOA
involved in memory IGI
IGI: Inferred from genetic interaction
11140685 GOA
involved in microglia development IGI
IGI: Inferred from genetic interaction
22198949 GOA
involved in microglial cell activation IDA
IDA: Inferred from direct assay
18723082 GOA
involved in microglial cell activation IGI
IGI: Inferred from genetic interaction
15457210 GOA
involved in modulation of excitatory postsynaptic potential IGI
IGI: Inferred from genetic interaction
19118188 GOA
involved in negative regulation of blood circulation IGI
IGI: Inferred from genetic interaction
12808450 GOA
involved in negative regulation of canonical Wnt signaling pathway IDA
IDA: Inferred from direct assay
18234671 GOA
involved in negative regulation of cell population proliferation IDA
IDA: Inferred from direct assay
22944668 GOA
involved in negative regulation of gene expression IDA
IDA: Inferred from direct assay
26006083 GOA
involved in negative regulation of gene expression IGI
IGI: Inferred from genetic interaction
18234671 GOA
involved in negative regulation of long-term synaptic potentiation IGI
IGI: Inferred from genetic interaction
15457210 GOA
involved in negative regulation of miRNA transcription IDA
IDA: Inferred from direct assay
24827165 GOA
involved in negative regulation of protein localization to nucleus IGI
IGI: Inferred from genetic interaction
18234671 GOA
involved in negative regulation of transcription by RNA polymerase II IGI
IGI: Inferred from genetic interaction
21803450 GOA
involved in neuron projection maintenance IGI
IGI: Inferred from genetic interaction
20445063 GOA
acts upstream of positive effect phospholipase D-activating G protein-coupled receptor signaling pathway IDA
IDA: Inferred from direct assay
18723082 GOA
involved in positive regulation of ERK1 and ERK2 cascade IDA
IDA: Inferred from direct assay
18723082 GOA
involved in positive regulation of ERK1 and ERK2 cascade IGI
IGI: Inferred from genetic interaction
15457210 GOA
involved in positive regulation of G protein-coupled receptor internalization IDA
IDA: Inferred from direct assay
18723082 GOA
involved in positive regulation of G protein-coupled receptor signaling pathway IDA
IDA: Inferred from direct assay
11316806 GOA
involved in positive regulation of JNK cascade IGI
IGI: Inferred from genetic interaction
23921129 GOA
involved in positive regulation of MAPK cascade IGI
IGI: Inferred from genetic interaction
15190117 GOA
involved in positive regulation of T cell migration IMP
IMP: Inferred from mutant phenotype
19660551 GOA
involved in positive regulation of Toll signaling pathway IGI
IGI: Inferred from genetic interaction
20037584 GOA
involved in positive regulation of amyloid fibril formation IMP
IMP: Inferred from mutant phenotype
19660551 GOA
involved in positive regulation of amyloid precursor protein catabolic process IGI
IGI: Inferred from genetic interaction
22406537 GOA
acts upstream of positive regulation of apoptotic process IDA
IDA: Inferred from direct assay
27241555 GOA
involved in positive regulation of apoptotic process IDA
IDA: Inferred from direct assay
11689470 GOA
involved in positive regulation of apoptotic process IGI
IGI: Inferred from genetic interaction
11689470 GOA
involved in positive regulation of cAMP/PKA signal transduction IDA
IDA: Inferred from direct assay
22500019 GOA
involved in positive regulation of calcium-mediated signaling IGI
IGI: Inferred from genetic interaction
22500019 GOA
involved in positive regulation of chemokine production IGI
IGI: Inferred from genetic interaction
22406537 GOA
involved in positive regulation of endothelin production IGI
IGI: Inferred from genetic interaction
12808450 GOA
involved in positive regulation of excitatory postsynaptic potential IGI
IGI: Inferred from genetic interaction
19118188 GOA
involved in positive regulation of extrinsic apoptotic signaling pathway IGI
IGI: Inferred from genetic interaction
20037584 GOA
involved in positive regulation of gene expression IDA
IDA: Inferred from direct assay
26006083 GOA
involved in positive regulation of gene expression IGI
IGI: Inferred from genetic interaction
20037584 GOA
involved in positive regulation of gene expression IMP
IMP: Inferred from mutant phenotype
15457210 GOA
involved in positive regulation of gene expression, epigenetic IGI
IGI: Inferred from genetic interaction
19057576 GOA
involved in positive regulation of glycolytic process IGI
IGI: Inferred from genetic interaction
29061364 GOA
involved in positive regulation of inflammatory response IMP
IMP: Inferred from mutant phenotype
29961672 GOA
involved in positive regulation of interleukin-1 beta production IGI
IGI: Inferred from genetic interaction
22406537 GOA
involved in positive regulation of interleukin-6 production IGI
IGI: Inferred from genetic interaction
22406537 GOA
involved in positive regulation of long-term synaptic potentiation IGI
IGI: Inferred from genetic interaction
19118188 GOA
involved in positive regulation of membrane protein ectodomain proteolysis IDA
IDA: Inferred from direct assay
25015123 GOA
involved in positive regulation of membrane protein ectodomain proteolysis IGI
IGI: Inferred from genetic interaction
25015123 GOA
involved in positive regulation of monocyte chemotaxis IDA
IDA: Inferred from direct assay
11160457 GOA
involved in positive regulation of monocyte chemotaxis IGI
IGI: Inferred from genetic interaction
11160457 GOA
involved in positive regulation of neuron apoptotic process IDA
IDA: Inferred from direct assay
29371969 GOA
involved in positive regulation of neuron apoptotic process IGI
IGI: Inferred from genetic interaction
23164821 GOA
involved in positive regulation of neuron differentiation IGI
IGI: Inferred from genetic interaction
15190117 GOA
involved in positive regulation of nitric oxide biosynthetic process IGI
IGI: Inferred from genetic interaction
20037584 GOA
involved in positive regulation of non-canonical NF-kappaB signal transduction IDA
IDA: Inferred from direct assay
22406537 GOA
involved in positive regulation of non-canonical NF-kappaB signal transduction IGI
IGI: Inferred from genetic interaction
15457210 GOA
involved in positive regulation of non-canonical NF-kappaB signal transduction IMP
IMP: Inferred from mutant phenotype
29961672 GOA
involved in positive regulation of peptidyl-serine phosphorylation IMP
IMP: Inferred from mutant phenotype
19660551 GOA
involved in positive regulation of peptidyl-threonine phosphorylation IMP
IMP: Inferred from mutant phenotype
19660551 GOA
NOT involved in positive regulation of peptidyl-tyrosine phosphorylation IDA
IDA: Inferred from direct assay
22635104 GOA
involved in positive regulation of protein import IDA
IDA: Inferred from direct assay
23164821 GOA
involved in positive regulation of protein metabolic process IMP
IMP: Inferred from mutant phenotype
11404397 GOA
involved in positive regulation of protein phosphorylation IDA
IDA: Inferred from direct assay
11404397 GOA
involved in positive regulation of protein phosphorylation IGI
IGI: Inferred from genetic interaction
15457210 GOA
involved in positive regulation of response to endoplasmic reticulum stress IDA
IDA: Inferred from direct assay
21803450 GOA
involved in positive regulation of superoxide anion generation IGI
IGI: Inferred from genetic interaction
11316806 GOA
involved in positive regulation of transcription by RNA polymerase II IGI
IGI: Inferred from genetic interaction
23921129 GOA
involved in positive regulation of tumor necrosis factor production IGI
IGI: Inferred from genetic interaction
12808450 GOA
involved in positive regulation of type II interferon production IGI
IGI: Inferred from genetic interaction
17255335 GOA
involved in protein homooligomerization IPI
IPI: Inferred from physical interaction
15447668 GOA
involved in protein tetramerization IMP
IMP: Inferred from mutant phenotype
19660551 GOA
involved in protein tetramerization IPI
IPI: Inferred from physical interaction
19660551 GOA
involved in protein trimerization IMP
IMP: Inferred from mutant phenotype
19660551 GOA
involved in protein trimerization IPI
IPI: Inferred from physical interaction
19660551 GOA
involved in regulation of amyloid fibril formation IGI
IGI: Inferred from genetic interaction
11140685 GOA
acts upstream of regulation of amyloid-beta clearance IMP
IMP: Inferred from mutant phenotype
19057576 GOA
NOT involved in regulation of calcium ion transmembrane transport via high voltage-gated calcium channel IDA
IDA: Inferred from direct assay
21883149 GOA
involved in regulation of dendritic spine maintenance IGI
IGI: Inferred from genetic interaction
23921129 GOA
involved in regulation of endoplasmic reticulum stress-induced neuron intrinsic apoptotic signaling pathway IGI
IGI: Inferred from genetic interaction
23921129 GOA
involved in regulation of gene expression IGI
IGI: Inferred from genetic interaction
21857966 GOA
acts upstream of or within regulation of gene expression IMP
IMP: Inferred from mutant phenotype
29274751 GOA
involved in regulation of long-term neuronal synaptic plasticity IGI
IGI: Inferred from genetic interaction
23921129 GOA
involved in regulation of neurotransmitter uptake IGI
IGI: Inferred from genetic interaction
19118188 GOA
involved in regulation of peptidyl-tyrosine phosphorylation IGI
IGI: Inferred from genetic interaction
21857966 GOA
involved in regulation of presynapse assembly IDA
IDA: Inferred from direct assay
19726636 GOA
involved in regulation of presynapse assembly IMP
IMP: Inferred from mutant phenotype
19726636 GOA
involved in regulation of spontaneous synaptic transmission IGI
IGI: Inferred from genetic interaction
15457210 GOA
involved in regulation of toll-like receptor signaling pathway IGI
IGI: Inferred from genetic interaction
20037584 GOA
involved in regulation of transcription by RNA polymerase II IGI
IGI: Inferred from genetic interaction
19057576 GOA
NOT involved in response to auditory stimulus IGI
IGI: Inferred from genetic interaction
19118188 GOA
involved in response to yeast IMP
IMP: Inferred from mutant phenotype
20209079 GOA
involved in synapse organization IGI
IGI: Inferred from genetic interaction
19587288 GOA
Cellular Component GO Annotation Evidence Références Source
located in Golgi apparatus IDA
IDA: Inferred from direct assay
14527950 GOA
part of amyloid-beta complex IMP
IMP: Inferred from mutant phenotype
23640054 GOA
part of amyloid-beta complex IPI
IPI: Inferred from physical interaction
22179788 GOA
colocalizes with cell body IDA
IDA: Inferred from direct assay
25390368 GOA
located in cell surface IDA
IDA: Inferred from direct assay
7593229 GOA
colocalizes with cytoplasm IDA
IDA: Inferred from direct assay
11689470 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
18509662 GOA
located in cytoplasm IGI
IGI: Inferred from genetic interaction
19808651 GOA
NOT colocalizes with dendrite IDA
IDA: Inferred from direct assay
17251419 GOA
is active in dendrite IDA
IDA: Inferred from direct assay
24012003 GOA
NOT colocalizes with dendrite membrane IDA
IDA: Inferred from direct assay
15537891 GOA
located in dendritic shaft IDA
IDA: Inferred from direct assay
11988176 GOA
located in dendritic spine IDA
IDA: Inferred from direct assay
11988176 GOA
located in early endosome IDA
IDA: Inferred from direct assay
14527950 GOA
located in endoplasmic reticulum IDA
IDA: Inferred from direct assay
14527950 GOA
located in endosome IDA
IDA: Inferred from direct assay
18353773 GOA
located in endosome to plasma membrane transport vesicle IDA
IDA: Inferred from direct assay
26005850 GOA
NOT located in external side of plasma membrane IDA
IDA: Inferred from direct assay
15537891 GOA
is active in extracellular space IDA
IDA: Inferred from direct assay
29518356 GOA
located in extracellular space IDA
IDA: Inferred from direct assay
20164328 GOA
located in extracellular space IMP
IMP: Inferred from mutant phenotype
23640054 GOA
part of high-density lipoprotein particle IDA
IDA: Inferred from direct assay
22138302 GOA
part of high-density lipoprotein particle IPI
IPI: Inferred from physical interaction
9211985 GOA
part of intermediate-density lipoprotein particle IDA
IDA: Inferred from direct assay
22138302 GOA
part of intermediate-density lipoprotein particle IPI
IPI: Inferred from physical interaction
9211985 GOA
part of lipoprotein particle IDA
IDA: Inferred from direct assay
22138302 GOA
part of low-density lipoprotein particle IPI
IPI: Inferred from physical interaction
9211985 GOA
colocalizes with lysosome IDA
IDA: Inferred from direct assay
21289173 GOA
located in membrane raft IDA
IDA: Inferred from direct assay
24499793 GOA
located in mitochondrion IDA
IDA: Inferred from direct assay
23525105 GOA
colocalizes with neuron projection IDA
IDA: Inferred from direct assay
25390368 GOA
located in nuclear envelope lumen IDA
IDA: Inferred from direct assay
21989385 GOA
located in nucleus IGI
IGI: Inferred from genetic interaction
19057576 GOA
located in perinuclear region of cytoplasm IDA
IDA: Inferred from direct assay
20427278 GOA
colocalizes with plasma membrane IDA
IDA: Inferred from direct assay
11689470 GOA
located in plasma membrane IDA
IDA: Inferred from direct assay
12805363 GOA
colocalizes with postsynapse IDA
IDA: Inferred from direct assay
25390368 GOA
colocalizes with presynapse IDA
IDA: Inferred from direct assay
25390368 GOA
part of protein-containing complex IDA
IDA: Inferred from direct assay
9228033 GOA
part of protein-containing complex IPI
IPI: Inferred from physical interaction
18568035 GOA
part of receptor complex IDA
IDA: Inferred from direct assay
23382219 GOA
located in synapse IDA
IDA: Inferred from direct assay
11988176 GOA
NOT colocalizes with synaptic membrane IDA
IDA: Inferred from direct assay
17308309 GOA
part of very-low-density lipoprotein particle IPI
IPI: Inferred from physical interaction
9211985 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

APP Protein Structure

APP_N

APP_N: Amyloid A4 N-terminal heparin-binding (31 - 131)

APP_Cu_bd

APP_Cu_bd: Copper-binding of amyloid precursor, CuBD (132 - 188)

Kunitz_BPTI

Kunitz_BPTI: Kunitz/Bovine pancreatic trypsin inhibitor domain (290 - 342)

APP_E2

APP_E2: E2 domain of amyloid precursor protein (366 - 549)

Beta-APP

Beta-APP: Beta-amyloid peptide (beta-APP) (675 - 713)

APP_amyloid

APP_amyloid: beta-amyloid precursor protein C-terminus (715 - 766)

  • 0
  • 200
  • 400
  • 600
  • 770 a.a.
Protein Preferred Names Protein Names

amyloid-beta precursor protein

  • alzheimer disease amyloid A4 protein homolog

  • alzheimer disease amyloid protein

  • amyloid beta (A4) precursor protein

  • amyloid beta A4 protein

  • amyloid precursor protein

  • beta-amyloid peptide

  • beta-amyloid peptide(1-40)

  • beta-amyloid peptide(1-42)

  • beta-amyloid precursor protein

  • cerebral vascular amyloid peptide

  • peptidase nexin-II

  • protease nexin-II

  • testicular tissue protein Li 2

APP Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Références
Intra
APP P05067 NEFL Homo sapiens I6L9F6 32814053
Intra
APP P05067 NEFL Homo sapiens I6L9F6 32814053
Intra
APP P05067 NEFL Homo sapiens I6L9F6 32814053
Intra
APP P05067 ARL16 Homo sapiens Q0P5N6 32814053
Intra
APP P05067 ARL16 Homo sapiens Q0P5N6 32814053
Intra
APP P05067 ARL16 Homo sapiens Q0P5N6 32814053
Intra
APP P05067 EPB41 Homo sapiens P11171-2 32814053
Intra
APP P05067 EPB41 Homo sapiens P11171-2 32814053
Intra
APP P05067 EPB41 Homo sapiens P11171-2 32814053
Intra
APP P05067 PLSCR1 Homo sapiens Q8WVK1 32814053
Intra
APP P05067 PLSCR1 Homo sapiens Q8WVK1 32814053
Intra
APP P05067 PLSCR1 Homo sapiens Q8WVK1 32814053
Intra
APP P05067 MARK4 Homo sapiens Q6IPE9 32814053
Intra
APP P05067 MARK4 Homo sapiens Q6IPE9 32814053
Intra
APP P05067 MARK4 Homo sapiens Q6IPE9 32814053
Intra
APP P05067 ARD1A Homo sapiens Q6P4J0 32814053
Intra
APP P05067 ARD1A Homo sapiens Q6P4J0 32814053
Intra
APP P05067 ARD1A Homo sapiens Q6P4J0 32814053
Intra
APP P05067 FKBP1A Homo sapiens P62942 32814053
Intra
APP P05067 FKBP1A Homo sapiens P62942 32814053
Intra
APP P05067 FKBP1A Homo sapiens P62942 32814053
Intra
APP P05067 PHF10 Homo sapiens Q8WUB8-2 32814053
Intra
APP P05067 PHF10 Homo sapiens Q8WUB8-2 32814053
Intra
APP P05067 PHF10 Homo sapiens Q8WUB8-2 32814053
Intra
APP P05067 NGF Homo sapiens P01138 32814053
Intra
APP P05067 NGF Homo sapiens P01138 32814053
Intra
APP P05067 NGF Homo sapiens P01138 32814053
Intra
APP P05067 PIK3CG Homo sapiens P48736 32814053
Intra
APP P05067 PIK3CG Homo sapiens P48736 32814053
Intra
APP P05067 PIK3CG Homo sapiens P48736 32814053
Intra
APP P05067 MMP2 Homo sapiens P08253 32814053
Intra
APP P05067 MMP2 Homo sapiens P08253 32814053
Intra
APP P05067 MMP2 Homo sapiens P08253 32814053
Intra
APP P05067 CDK5 Homo sapiens Q00535 32814053
Intra
APP P05067 CDK5 Homo sapiens Q00535 32814053
Intra
APP P05067 CDK5 Homo sapiens Q00535 32814053
Intra
APP P05067 PDIA6 Homo sapiens Q15084 32814053
Intra
APP P05067 PDIA6 Homo sapiens Q15084 32814053
Intra
APP P05067 PDIA6 Homo sapiens Q15084 32814053
Intra
APP P05067 CORO1A Homo sapiens P31146 32814053
Intra
APP P05067 CORO1A Homo sapiens P31146 32814053
Intra
APP P05067 CORO1A Homo sapiens P31146 32814053
Intra
APP P05067 SUPT16H Homo sapiens Q9Y5B9 32814053
Intra
APP P05067 SUPT16H Homo sapiens Q9Y5B9 32814053
Intra
APP P05067 SUPT16H Homo sapiens Q9Y5B9 32814053
Intra
APP P05067 TBR1 Homo sapiens Q16650 32814053
Intra
APP P05067 TBR1 Homo sapiens Q16650 32814053
Intra
APP P05067 TBR1 Homo sapiens Q16650 32814053
Intra
APP P05067 SEPTIN4 Homo sapiens O43236 32814053
Intra
APP P05067 SEPTIN4 Homo sapiens O43236 32814053
Intra
APP P05067 SEPTIN4 Homo sapiens O43236 32814053
Intra
APP P05067 FGF14 Homo sapiens Q92915 32814053
Intra
APP P05067 FGF14 Homo sapiens Q92915 32814053
Intra
APP P05067 FGF14 Homo sapiens Q92915 32814053
Intra
APP P05067 PPP2R2A Homo sapiens P63151 32814053
Intra
APP P05067 PPP2R2A Homo sapiens P63151 32814053
Intra
APP P05067 PPP2R2A Homo sapiens P63151 32814053
Intra
APP P05067 CALR Homo sapiens P27797 15896298
Intra
APP P05067 CALR Homo sapiens P27797 32814053
Intra
APP P05067 CALR Homo sapiens P27797 32814053
Intra
APP P05067 CALR Homo sapiens P27797 32814053
Intra
APP P05067 LRPPRC Homo sapiens P42704 25959826
Intra
APP P05067 LRPPRC Homo sapiens P42704 25959826
Intra
APP P05067 CNTF Homo sapiens P26441 32814053
Intra
APP P05067 CNTF Homo sapiens P26441 32814053
Intra
APP P05067 CNTF Homo sapiens P26441 32814053
Intra
APP P05067 PPP2R2B Homo sapiens Q00005 32814053
Intra
APP P05067 PPP2R2B Homo sapiens Q00005 32814053
Intra
APP P05067 PPP2R2B Homo sapiens Q00005 32814053
Intra
APP P05067 VPS35 Homo sapiens Q96QK1 32814053
Intra
APP P05067 VPS35 Homo sapiens Q96QK1 32814053
Intra
APP P05067 VPS35 Homo sapiens Q96QK1 32814053
Intra
APP P05067 GTF3C3 Homo sapiens Q9Y5Q9 32814053
Intra
APP P05067 GTF3C3 Homo sapiens Q9Y5Q9 32814053
Intra
APP P05067 GTF3C3 Homo sapiens Q9Y5Q9 32814053
Intra
APP P05067 CLPP Homo sapiens Q16740 32814053
Intra
APP P05067 CLPP Homo sapiens Q16740 32814053
Intra
APP P05067 CLPP Homo sapiens Q16740 32814053
Intra
APP P05067 PPP1R2 Homo sapiens P41236 32814053
Intra
APP P05067 PPP1R2 Homo sapiens P41236 32814053
Intra
APP P05067 PPP1R2 Homo sapiens P41236 32814053
Intra
APP P05067 FURIN Homo sapiens P09958 32814053
Intra
APP P05067 FURIN Homo sapiens P09958 32814053
Intra
APP P05067 FURIN Homo sapiens P09958 32814053
Intra
APP P05067 MAP2K2 Homo sapiens P36507 32814053
Intra
APP P05067 MAP2K2 Homo sapiens P36507 32814053
Intra
APP P05067 MAP2K2 Homo sapiens P36507 32814053
Intra
APP P05067 OTUB1 Homo sapiens Q96FW1 32814053
Intra
APP P05067 OTUB1 Homo sapiens Q96FW1 32814053
Intra
APP P05067 OTUB1 Homo sapiens Q96FW1 32814053
Intra
APP P05067 STAT3 Homo sapiens P40763-2 32814053
Intra
APP P05067 STAT3 Homo sapiens P40763-2 32814053
Intra
APP P05067 STAT3 Homo sapiens P40763-2 32814053
Intra
APP P05067 BAG6 Homo sapiens P46379-2 32814053
Intra
APP P05067 BAG6 Homo sapiens P46379-2 32814053
Intra
APP P05067 BAG6 Homo sapiens P46379-2 32814053
Intra
APP P05067 CLU Homo sapiens P10909 32814053
Intra
APP P05067 CLU Homo sapiens P10909 32814053
Intra
APP P05067 CLU Homo sapiens P10909 32814053
Intra
APP P05067 PSEN1 Homo sapiens P49768-2 32814053
Intra
APP P05067 PSEN1 Homo sapiens P49768-2 32814053
Intra
APP P05067 PSEN1 Homo sapiens P49768-2 32814053
Intra
APP P05067 LDHAL6B Homo sapiens Q9BYZ2 32814053
Intra
APP P05067 LDHAL6B Homo sapiens Q9BYZ2 32814053
Intra
APP P05067 LDHAL6B Homo sapiens Q9BYZ2 32814053
Intra
APP P05067 BACE2 Homo sapiens Q9Y5Z0 32814053
Intra
APP P05067 BACE2 Homo sapiens Q9Y5Z0 32814053
Intra
APP P05067 BACE2 Homo sapiens Q9Y5Z0 32814053
Intra
APP P05067 SIAH1 Homo sapiens Q8IUQ4-2 32814053
Intra
APP P05067 SIAH1 Homo sapiens Q8IUQ4-2 32814053
Intra
APP P05067 SIAH1 Homo sapiens Q8IUQ4-2 32814053
Intra
APP P05067 SEPTIN2 Homo sapiens Q15019-3 32814053
Intra
APP P05067 SEPTIN2 Homo sapiens Q15019-3 32814053
Intra
APP P05067 SEPTIN2 Homo sapiens Q15019-3 32814053
Intra
APP P05067 AP2B1 Homo sapiens P63010-2 32814053
Intra
APP P05067 AP2B1 Homo sapiens P63010-2 32814053
Intra
APP P05067 AP2B1 Homo sapiens P63010-2 32814053
Intra
APP P05067 PARK7 Homo sapiens Q99497 32814053
Intra
APP P05067 PARK7 Homo sapiens Q99497 32814053
Intra
APP P05067 PARK7 Homo sapiens Q99497 32814053
Intra
APP P05067 DAB2 Homo sapiens P98082 32814053
Intra
APP P05067 DAB2 Homo sapiens P98082 32814053
Intra
APP P05067 DAB2 Homo sapiens P98082 32814053
Intra
APP P05067 SORL1 Homo sapiens Q92673 32814053
Intra
APP P05067 SORL1 Homo sapiens Q92673 32814053
Intra
APP P05067 SORL1 Homo sapiens Q92673 32814053
Intra
APP P05067 WT1 Homo sapiens P19544-6 32814053
Intra
APP P05067 WT1 Homo sapiens P19544-6 32814053
Intra
APP P05067 WT1 Homo sapiens P19544-6 32814053
Intra
APP P05067 TP53BP2 Homo sapiens Q05BL1 32814053
Intra
APP P05067 TP53BP2 Homo sapiens Q05BL1 32814053
Intra
APP P05067 TP53BP2 Homo sapiens Q05BL1 32814053
Intra
APP P05067 FBLN1 Homo sapiens P23142-4 32814053
Intra
APP P05067 FBLN1 Homo sapiens P23142-4 32814053
Intra
APP P05067 FBLN1 Homo sapiens P23142-4 32814053
Intra
APP P05067 SPAG8 Homo sapiens Q99932-2 32814053
Intra
APP P05067 SPAG8 Homo sapiens Q99932-2 32814053
Intra
APP P05067 SPAG8 Homo sapiens Q99932-2 32814053
Intra
APP P05067 KLC1 Homo sapiens Q07866-2 32814053
Intra
APP P05067 KLC1 Homo sapiens Q07866-2 32814053
Intra
APP P05067 KLC1 Homo sapiens Q07866-2 32814053
Intra
APP P05067 TSC22D1 Homo sapiens Q15714-2 32814053
Intra
APP P05067 TSC22D1 Homo sapiens Q15714-2 32814053
Intra
APP P05067 TSC22D1 Homo sapiens Q15714-2 32814053
Intra
APP P05067 GGA1 Homo sapiens Q9UJY5-4 32814053
Intra
APP P05067 GGA1 Homo sapiens Q9UJY5-4 32814053
Intra
APP P05067 GGA1 Homo sapiens Q9UJY5-4 32814053
Intra
APP P05067 NBL1 Homo sapiens P41271-2 32814053
Intra
APP P05067 NBL1 Homo sapiens P41271-2 32814053
Intra
APP P05067 NBL1 Homo sapiens P41271-2 32814053
Intra
APP P05067 TMEM121 Homo sapiens Q9BTD3 32814053
Intra
APP P05067 TMEM121 Homo sapiens Q9BTD3 32814053
Intra
APP P05067 TMEM121 Homo sapiens Q9BTD3 32814053
Intra
APP P05067 ZNF92 Homo sapiens Q03936 33961781
Intra
APP P05067 ZNF92 Homo sapiens Q03936 35914814
Intra
APP P05067 ZNF92 Homo sapiens Q03936 31413325
Intra
APP P05067 COL4A5 Homo sapiens P29400-2 32814053
Intra
APP P05067 COL4A5 Homo sapiens P29400-2 32814053
Intra
APP P05067 COL4A5 Homo sapiens P29400-2 32814053
Intra
APP P05067 CASP1 Homo sapiens P29466-3 32814053
Intra
APP P05067 CASP1 Homo sapiens P29466-3 32814053
Intra
APP P05067 CASP1 Homo sapiens P29466-3 32814053
Intra
APP P05067 BDNF Homo sapiens P23560-2 32814053
Intra
APP P05067 BDNF Homo sapiens P23560-2 32814053
Intra
APP P05067 BDNF Homo sapiens P23560-2 32814053
Intra
APP P05067 TGIF1 Homo sapiens Q15583-2 32814053
Intra
APP P05067 TGIF1 Homo sapiens Q15583-2 32814053
Intra
APP P05067 TGIF1 Homo sapiens Q15583-2 32814053
Intra
APP P05067 STH Homo sapiens Q8IWL8 32814053
Intra
APP P05067 STH Homo sapiens Q8IWL8 32814053
Intra
APP P05067 STH Homo sapiens Q8IWL8 32814053
Intra
APP P05067 APBB1 Homo sapiens O00213-2 32814053
Intra
APP P05067 APBB1 Homo sapiens O00213-2 32814053
Intra
APP P05067 APBB1 Homo sapiens O00213-2 32814053
Intra
APP P05067 PDGFRA Homo sapiens P16234-2 32814053
Intra
APP P05067 PDGFRA Homo sapiens P16234-2 32814053
Intra
APP P05067 PDGFRA Homo sapiens P16234-2 32814053
Intra
APP P05067 CAMK2A Homo sapiens Q9UQM7 32814053
Intra
APP P05067 CAMK2A Homo sapiens Q9UQM7 32814053
Intra
APP P05067 CAMK2A Homo sapiens Q9UQM7 32814053
Intra
APP P05067 RPS6KA2 Homo sapiens Q15349 32814053
Intra
APP P05067 RPS6KA2 Homo sapiens Q15349 32814053
Intra
APP P05067 RPS6KA2 Homo sapiens Q15349 32814053
Intra
APP P05067 NGFR Homo sapiens P08138 19225519
Intra
APP P05067 NGFR Homo sapiens P08138 19225519
Intra
APP P05067 ADAM10 Homo sapiens O14672 30538620
Intra
APP P05067 CAPN1 Homo sapiens P07384 32814053
Intra
APP P05067 CAPN1 Homo sapiens P07384 32814053
Intra
APP P05067 CAPN1 Homo sapiens P07384 32814053
Intra
APP P05067 GSK3B Homo sapiens P49841-2 32814053
Intra
APP P05067 GSK3B Homo sapiens P49841-2 32814053
Intra
APP P05067 GSK3B Homo sapiens P49841-2 32814053
Intra
APP P05067 LRP1B Homo sapiens Q9NZR2 32814053
Intra
APP P05067 LRP1B Homo sapiens Q9NZR2 32814053
Intra
APP P05067 LRP1B Homo sapiens Q9NZR2 32814053
Intra
APP P05067 AGER Homo sapiens Q15109 32814053
Intra
APP P05067 AGER Homo sapiens Q15109 32814053
Intra
APP P05067 AGER Homo sapiens Q15109 32814053
Intra
APP P05067 ADCYAP1R1 Homo sapiens P41586-2 32814053
Intra
APP P05067 ADCYAP1R1 Homo sapiens P41586-2 32814053
Intra
APP P05067 ADCYAP1R1 Homo sapiens P41586-2 32814053
Intra
APP P05067 CD47 Homo sapiens Q08722-3 32814053
Intra
APP P05067 CD47 Homo sapiens Q08722-3 32814053
Intra
APP P05067 CD47 Homo sapiens Q08722-3 32814053
Intra
APP P05067 FPR2 Homo sapiens P25090 32814053
Intra
APP P05067 FPR2 Homo sapiens P25090 32814053
Intra
APP P05067 FPR2 Homo sapiens P25090 32814053
Intra
APP P05067 SNX17 Homo sapiens Q15036 32814053
Intra
APP P05067 SNX17 Homo sapiens Q15036 32814053
Intra
APP P05067 SNX17 Homo sapiens Q15036 32814053
Intra
APP P05067 LAMA4 Homo sapiens Q16363-3 32814053
Intra
APP P05067 LAMA4 Homo sapiens Q16363-3 32814053
Intra
APP P05067 LAMA4 Homo sapiens Q16363-3 32814053
Intra
APP P05067 CALHM1 Homo sapiens Q8IU99 32814053
Intra
APP P05067 CALHM1 Homo sapiens Q8IU99 32814053
Intra
APP P05067 CALHM1 Homo sapiens Q8IU99 32814053
Intra
APP P05067 PSEN2 Homo sapiens P49810 32814053
Intra
APP P05067 PSEN2 Homo sapiens P49810 32814053
Intra
APP P05067 PSEN2 Homo sapiens P49810 32814053
Cross
APP P05067 Slc5a7 Mus musculus Q8BGY9 17709753
Intra
APP P05067 KAT5 Homo sapiens Q92993-2 32814053
Intra
APP P05067 KAT5 Homo sapiens Q92993-2 32814053
Intra
APP P05067 KAT5 Homo sapiens Q92993-2 32814053
Intra
APP P05067 SST Homo sapiens P61278 32814053
Intra
APP P05067 SST Homo sapiens P61278 32814053
Intra
APP P05067 SST Homo sapiens P61278 32814053
Intra
APP P05067 CTSD Homo sapiens P07339 17112520
Intra
APP P05067 RNF111 Homo sapiens Q6ZNA4-2 32814053
Intra
APP P05067 RNF111 Homo sapiens Q6ZNA4-2 32814053
Intra
APP P05067 RNF111 Homo sapiens Q6ZNA4-2 32814053
Intra
APP P05067 APBB2 Homo sapiens Q92870-2 32814053
Intra
APP P05067 APBB2 Homo sapiens Q92870-2 32814053
Intra
APP P05067 APBB2 Homo sapiens Q92870-2 32814053
Intra
APP P05067 COL26A1 Homo sapiens Q96A83-2 32814053
Intra
APP P05067 COL26A1 Homo sapiens Q96A83-2 32814053
Intra
APP P05067 COL26A1 Homo sapiens Q96A83-2 32814053
Intra
APP P05067 SCARA3 Homo sapiens Q6AZY7-2 32814053
Intra
APP P05067 SCARA3 Homo sapiens Q6AZY7-2 32814053
Intra
APP P05067 SCARA3 Homo sapiens Q6AZY7-2 32814053
Intra
APP P05067 IQSEC1 Homo sapiens Q6DN90-2 32814053
Intra
APP P05067 IQSEC1 Homo sapiens Q6DN90-2 32814053
Intra
APP P05067 IQSEC1 Homo sapiens Q6DN90-2 32814053
Intra
APP P05067 FLOT2 Homo sapiens Q9BTI6 32814053
Intra
APP P05067 FLOT2 Homo sapiens Q9BTI6 32814053
Intra
APP P05067 FLOT2 Homo sapiens Q9BTI6 32814053
Intra
APP P05067 KLK6 Homo sapiens Q92876 32814053
Intra
APP P05067 KLK6 Homo sapiens Q92876 32814053
Intra
APP P05067 KLK6 Homo sapiens Q92876 32814053
Intra
APP P05067 COL4A6 Homo sapiens Q14031 32814053
Intra
APP P05067 COL4A6 Homo sapiens Q14031 32814053
Intra
APP P05067 COL4A6 Homo sapiens Q14031 32814053
Intra
APP P05067 BACE1 Homo sapiens P56817 30538620
Intra
APP P05067 BACE1 Homo sapiens P56817 32814053
Intra
APP P05067 BACE1 Homo sapiens P56817 32814053
Intra
APP P05067 BACE1 Homo sapiens P56817 32814053
Intra
APP P05067 BACE1 Homo sapiens P56817
Y2H
12901838
Intra
APP P05067 SNX33 Homo sapiens Q8WV41 32814053
Intra
APP P05067 SNX33 Homo sapiens Q8WV41 32814053
Intra
APP P05067 SNX33 Homo sapiens Q8WV41 32814053
Intra
APP P05067 MPND Homo sapiens Q8N594 32814053
Intra
APP P05067 MPND Homo sapiens Q8N594 32814053
Intra
APP P05067 MPND Homo sapiens Q8N594 32814053
Intra
APP P05067 VPS33A Homo sapiens Q96AX1 32814053
Intra
APP P05067 VPS33A Homo sapiens Q96AX1 32814053
Intra
APP P05067 VPS33A Homo sapiens Q96AX1 32814053
Intra
APP P05067 IDE Homo sapiens P14735 32814053
Intra
APP P05067 IDE Homo sapiens P14735 32814053
Intra
APP P05067 IDE Homo sapiens P14735 32814053
Intra
APP P05067 APLP2 Homo sapiens Q06481-5 32814053
Intra
APP P05067 APLP2 Homo sapiens Q06481-5 32814053
Intra
APP P05067 APLP2 Homo sapiens Q06481-5 32814053
Intra
APP P05067 RNF112 Homo sapiens Q9ULX5 32814053
Intra
APP P05067 RNF112 Homo sapiens Q9ULX5 32814053
Intra
APP P05067 RNF112 Homo sapiens Q9ULX5 32814053
Intra
APP P05067 TM2D1 Homo sapiens Q9BX74 32814053
Intra
APP P05067 TM2D1 Homo sapiens Q9BX74 32814053
Intra
APP P05067 TM2D1 Homo sapiens Q9BX74 32814053
Intra
APP P05067 CLSTN3 Homo sapiens Q8IUW6 32814053
Intra
APP P05067 CLSTN3 Homo sapiens Q8IUW6 32814053
Intra
APP P05067 CLSTN3 Homo sapiens Q8IUW6 32814053
Intra
APP P05067 LRP1 Homo sapiens Q07954-2 32814053
Intra
APP P05067 LRP1 Homo sapiens Q07954-2 32814053
Intra
APP P05067 LRP1 Homo sapiens Q07954-2 32814053
Intra
APP P05067 UNG Homo sapiens P13051-2 32814053
Intra
APP P05067 UNG Homo sapiens P13051-2 32814053
Intra
APP P05067 UNG Homo sapiens P13051-2 32814053
Intra
APP P05067 COL25A1 Homo sapiens Q8NE08 32814053
Intra
APP P05067 COL25A1 Homo sapiens Q8NE08 32814053
Intra
APP P05067 COL25A1 Homo sapiens Q8NE08 32814053
Intra
APP P05067 DCTN1 Homo sapiens Q14203-5 32814053
Intra
APP P05067 DCTN1 Homo sapiens Q14203-5 32814053
Intra
APP P05067 DCTN1 Homo sapiens Q14203-5 32814053
Intra
APP P05067 EPB41 Homo sapiens P11171-7 32814053
Intra
APP P05067 EPB41 Homo sapiens P11171-7 32814053
Intra
APP P05067 EPB41 Homo sapiens P11171-7 32814053
Intra
APP P05067 NOTCH1 Homo sapiens Q6IAD4 32814053
Intra
APP P05067 NOTCH1 Homo sapiens Q6IAD4 32814053
Intra
APP P05067 NOTCH1 Homo sapiens Q6IAD4 32814053
Intra
APP P05067 RPS6KB1 Homo sapiens P23443-4 32814053
Intra
APP P05067 RPS6KB1 Homo sapiens P23443-4 32814053
Intra
APP P05067 RPS6KB1 Homo sapiens P23443-4 32814053
Intra
APP P05067 CANX Homo sapiens P27824-2 32814053
Intra
APP P05067 CANX Homo sapiens P27824-2 32814053
Intra
APP P05067 CANX Homo sapiens P27824-2 32814053
Intra
APP P05067 SEPTIN8 Homo sapiens Q92599-3 32814053
Intra
APP P05067 SEPTIN8 Homo sapiens Q92599-3 32814053
Intra
APP P05067 SEPTIN8 Homo sapiens Q92599-3 32814053
Intra
APP P05067 VPS29 Homo sapiens Q8N0S8 32814053
Intra
APP P05067 VPS29 Homo sapiens Q8N0S8 32814053
Intra
APP P05067 VPS29 Homo sapiens Q8N0S8 32814053
Intra
APP P05067 SYK Homo sapiens P43405-2 32814053
Intra
APP P05067 SYK Homo sapiens P43405-2 32814053
Intra
APP P05067 SYK Homo sapiens P43405-2 32814053
Intra
APP P05067 DKFZP586N0721 Homo sapiens Q6I9W9 32814053
Intra
APP P05067 DKFZP586N0721 Homo sapiens Q6I9W9 32814053
Intra
APP P05067 DKFZP586N0721 Homo sapiens Q6I9W9 32814053
Intra
APP P05067 CPB1 Homo sapiens P15086 32814053
Intra
APP P05067 CPB1 Homo sapiens P15086 32814053
Intra
APP P05067 CPB1 Homo sapiens P15086 32814053
Intra
APP P05067 PRKACB Homo sapiens P22694-8 32814053
Intra
APP P05067 PRKACB Homo sapiens P22694-8 32814053
Intra
APP P05067 PRKACB Homo sapiens P22694-8 32814053
Intra
APP P05067 NUMB Homo sapiens P49757-8 32814053
Intra
APP P05067 NUMB Homo sapiens P49757-8 32814053
Intra
APP P05067 NUMB Homo sapiens P49757-8 32814053
Intra
APP P05067 STX5 Homo sapiens Q13190-4 32814053
Intra
APP P05067 STX5 Homo sapiens Q13190-4 32814053
Intra
APP P05067 STX5 Homo sapiens Q13190-4 32814053
Intra
APP P05067 NRG1 Homo sapiens Q6PK61 32814053
Intra
APP P05067 NRG1 Homo sapiens Q6PK61 32814053
Intra
APP P05067 NRG1 Homo sapiens Q6PK61 32814053
Intra
APP P05067 q8nht4_human Homo sapiens Q8NHT4 32814053
Intra
APP P05067 q8nht4_human Homo sapiens Q8NHT4 32814053
Intra
APP P05067 q8nht4_human Homo sapiens Q8NHT4 32814053
Intra
APP P05067 HSD17B10 Homo sapiens Q99714-2 32814053
Intra
APP P05067 HSD17B10 Homo sapiens Q99714-2 32814053
Intra
APP P05067 HSD17B10 Homo sapiens Q99714-2 32814053
Intra
APP P05067 PRKAG2 Homo sapiens Q9UGJ0-3 32814053
Intra
APP P05067 PRKAG2 Homo sapiens Q9UGJ0-3 32814053
Intra
APP P05067 PRKAG2 Homo sapiens Q9UGJ0-3 32814053
Intra
APP P05067 APH1B Homo sapiens Q8WW43 32814053
Intra
APP P05067 APH1B Homo sapiens Q8WW43 32814053
Intra
APP P05067 APH1B Homo sapiens Q8WW43 32814053
Intra
APP P05067 APH1A Homo sapiens Q96BI3 32814053
Intra
APP P05067 APH1A Homo sapiens Q96BI3 32814053
Intra
APP P05067 APH1A Homo sapiens Q96BI3 32814053
Intra
APP P05067 PIK3CB Homo sapiens P42338 32814053
Intra
APP P05067 PIK3CB Homo sapiens P42338 32814053
Intra
APP P05067 PIK3CB Homo sapiens P42338 32814053
Intra
APP P05067 NUCB1 Homo sapiens Q02818 32814053
Intra
APP P05067 NUCB1 Homo sapiens Q02818 32814053
Intra
APP P05067 NUCB1 Homo sapiens Q02818 32814053
Intra
APP P05067 PRKACB Homo sapiens P22694 32814053
Intra
APP P05067 PRKACB Homo sapiens P22694 32814053
Intra
APP P05067 PRKACB Homo sapiens P22694 32814053
Intra
APP P05067 NR4A2 Homo sapiens P43354 32814053
Intra
APP P05067 NR4A2 Homo sapiens P43354 32814053
Intra
APP P05067 NR4A2 Homo sapiens P43354 32814053
Intra
APP P05067 JUND Homo sapiens P17535 32814053
Intra
APP P05067 JUND Homo sapiens P17535 32814053
Intra
APP P05067 JUND Homo sapiens P17535 32814053
Intra
APP P05067 BCAN Homo sapiens Q96GW7 32814053
Intra
APP P05067 BCAN Homo sapiens Q96GW7 32814053
Intra
APP P05067 BCAN Homo sapiens Q96GW7 32814053
Intra
APP P05067 CD36 Homo sapiens P16671 32814053
Intra
APP P05067 CD36 Homo sapiens P16671 32814053
Intra
APP P05067 CD36 Homo sapiens P16671 32814053
Intra
APP P05067 ZNF366 Homo sapiens Q8N895 32814053
Intra
APP P05067 ZNF366 Homo sapiens Q8N895 32814053
Intra
APP P05067 ZNF366 Homo sapiens Q8N895 32814053
Intra
APP P05067 PPP3CC Homo sapiens P48454 32814053
Intra
APP P05067 PPP3CC Homo sapiens P48454 32814053
Intra
APP P05067 PPP3CC Homo sapiens P48454 32814053
Intra
APP P05067 PLD1 Homo sapiens Q13393 32814053
Intra
APP P05067 PLD1 Homo sapiens Q13393 32814053
Intra
APP P05067 PLD1 Homo sapiens Q13393 32814053
Intra
APP P05067 TMEM30A Homo sapiens Q9NV96 30086173
Intra
APP P05067 PINK1 Homo sapiens Q9BXM7 32814053
Intra
APP P05067 PINK1 Homo sapiens Q9BXM7 32814053
Intra
APP P05067 PINK1 Homo sapiens Q9BXM7 32814053
Intra
APP P05067 SDC1 Homo sapiens P18827 32814053
Intra
APP P05067 SDC1 Homo sapiens P18827 32814053
Intra
APP P05067 SDC1 Homo sapiens P18827 32814053
Intra
APP P05067 APBB3 Homo sapiens O95704 31413325
Intra
APP P05067 APBB3 Homo sapiens O95704 35914814
Intra
APP P05067 ITM2B Homo sapiens Q9Y287 32814053
Intra
APP P05067 ITM2B Homo sapiens Q9Y287 32814053
Intra
APP P05067 ITM2B Homo sapiens Q9Y287 32814053
Intra
APP P05067 ITM2B Homo sapiens Q9Y287 34446781
Intra
APP P05067 EDRF1 Homo sapiens Q3B7T1 32814053
Intra
APP P05067 EDRF1 Homo sapiens Q3B7T1 32814053
Intra
APP P05067 EDRF1 Homo sapiens Q3B7T1 32814053
Intra
APP P05067 NEFH Homo sapiens P12036 32814053
Intra
APP P05067 NEFH Homo sapiens P12036 32814053
Intra
APP P05067 NEFH Homo sapiens P12036 32814053
Intra
APP P05067 HSP90AA1 Homo sapiens P07900 32814053
Intra
APP P05067 HSP90AA1 Homo sapiens P07900 32814053
Intra
APP P05067 HSP90AA1 Homo sapiens P07900 32814053
Intra
APP P05067 HSP90AA1 Homo sapiens P07900 16049941
Intra
APP P05067 PSEN1 Homo sapiens P49768 21163940
Intra
APP P05067 PTK2B Homo sapiens Q14289 32814053
Intra
APP P05067 PTK2B Homo sapiens Q14289 32814053
Intra
APP P05067 PTK2B Homo sapiens Q14289 32814053
Intra
APP P05067 MARK4 Homo sapiens Q96L34 32814053
Intra
APP P05067 MARK4 Homo sapiens Q96L34 32814053
Intra
APP P05067 MARK4 Homo sapiens Q96L34 32814053
Intra
APP P05067 TUBA1A Homo sapiens Q71U36 32814053
Intra
APP P05067 TUBA1A Homo sapiens Q71U36 32814053
Intra
APP P05067 TUBA1A Homo sapiens Q71U36 32814053
Intra
APP P05067 SQSTM1 Homo sapiens Q13501 32814053
Intra
APP P05067 SQSTM1 Homo sapiens Q13501 32814053
Intra
APP P05067 SQSTM1 Homo sapiens Q13501 32814053
Intra
APP P05067 SMAD3 Homo sapiens P84022 32814053
Intra
APP P05067 SMAD3 Homo sapiens P84022 32814053
Intra
APP P05067 SMAD3 Homo sapiens P84022 32814053
Intra
APP P05067 SMAD4 Homo sapiens Q13485 32814053
Intra
APP P05067 SMAD4 Homo sapiens Q13485 32814053
Intra
APP P05067 SMAD4 Homo sapiens Q13485 32814053
Intra
APP P05067 UBE2D2 Homo sapiens P62837 32814053
Intra
APP P05067 UBE2D2 Homo sapiens P62837 32814053
Intra
APP P05067 UBE2D2 Homo sapiens P62837 32814053
Intra
APP P05067 CSNK2A1 Homo sapiens P68400 32814053
Intra
APP P05067 CSNK2A1 Homo sapiens P68400 32814053
Intra
APP P05067 CSNK2A1 Homo sapiens P68400 32814053
Intra
APP P05067 TUBB Homo sapiens P07437 32814053
Intra
APP P05067 TUBB Homo sapiens P07437 32814053
Intra
APP P05067 TUBB Homo sapiens P07437 16049941
Intra
APP P05067 TUBB Homo sapiens P07437 32814053
Intra
APP P05067 ACTR3 Homo sapiens P61158 32814053
Intra
APP P05067 ACTR3 Homo sapiens P61158 32814053
Intra
APP P05067 ACTR3 Homo sapiens P61158 32814053
Intra
APP P05067 TUBA4A Homo sapiens P68366 32814053
Intra
APP P05067 TUBA4A Homo sapiens P68366 32814053
Intra
APP P05067 TUBA4A Homo sapiens P68366 32814053
Intra
APP P05067 HSPA8 Homo sapiens P11142 32814053
Intra
APP P05067 HSPA8 Homo sapiens P11142 32814053
Intra
APP P05067 HSPA8 Homo sapiens P11142 16049941
Intra
APP P05067 HSPA8 Homo sapiens P11142 32814053
Intra
APP P05067 HSPD1 Homo sapiens P10809 32814053
Intra
APP P05067 HSPD1 Homo sapiens P10809 32814053
Intra
APP P05067 HSPD1 Homo sapiens P10809 32814053
Intra
APP P05067 MME Homo sapiens P08473 32814053
Intra
APP P05067 MME Homo sapiens P08473 32814053
Intra
APP P05067 MME Homo sapiens P08473 32814053
Intra
APP P05067 ACTB Homo sapiens P60709 32814053
Intra
APP P05067 ACTB Homo sapiens P60709 16049941
Intra
APP P05067 ACTB Homo sapiens P60709 32814053
Intra
APP P05067 ACTB Homo sapiens P60709 32814053
Intra
APP P05067 HSPA5 Homo sapiens P11021 32814053
Intra
APP P05067 HSPA5 Homo sapiens P11021 33961781
Intra
APP P05067 HSPA5 Homo sapiens P11021 32814053
Intra
APP P05067 HSPA5 Homo sapiens P11021 32814053
Intra
APP P05067 TBP Homo sapiens P20226 32814053
Intra
APP P05067 TBP Homo sapiens P20226 32814053
Intra
APP P05067 TBP Homo sapiens P20226 32814053
Intra
APP P05067 CCT6A Homo sapiens P40227 32814053
Intra
APP P05067 CCT6A Homo sapiens P40227 32814053
Intra
APP P05067 CCT6A Homo sapiens P40227 32814053
Intra
APP P05067 PPP1CA Homo sapiens P62136 32814053
Intra
APP P05067 PPP1CA Homo sapiens P62136 32814053
Intra
APP P05067 PPP1CA Homo sapiens P62136 32814053
Intra
APP P05067 SKIC8 Homo sapiens Q9GZS3 32814053
Intra
APP P05067 SKIC8 Homo sapiens Q9GZS3 32814053
Intra
APP P05067 SKIC8 Homo sapiens Q9GZS3 32814053
Intra
APP P05067 HSP90B1 Homo sapiens P14625 32814053
Intra
APP P05067 HSP90B1 Homo sapiens P14625 32814053
Intra
APP P05067 HSP90B1 Homo sapiens P14625 32814053
Intra
APP P05067 PSMC3 Homo sapiens P17980 32814053
Intra
APP P05067 PSMC3 Homo sapiens P17980 32814053
Intra
APP P05067 PSMC3 Homo sapiens P17980 32814053
Intra
APP P05067 YWHAB Homo sapiens P31946 32814053
Intra
APP P05067 YWHAB Homo sapiens P31946 32814053
Intra
APP P05067 YWHAB Homo sapiens P31946 32814053
Intra
APP P05067 MAPT Homo sapiens P10636 16446437
Intra
APP P05067 MAPT Homo sapiens P10636 32814053
Intra
APP P05067 MAPT Homo sapiens P10636 32814053
Intra
APP P05067 MAPT Homo sapiens P10636 32814053
Intra
APP P05067 MAPT Homo sapiens P10636-8 16446437
Intra
APP P05067 INA Homo sapiens Q16352 32814053
Intra
APP P05067 INA Homo sapiens Q16352 32814053
Intra
APP P05067 INA Homo sapiens Q16352 32814053
Intra
APP P05067 RPL28 Homo sapiens P46779 32814053
Intra
APP P05067 RPL28 Homo sapiens P46779 32814053
Intra
APP P05067 RPL28 Homo sapiens P46779 32814053
Intra
APP P05067 APBA1 Homo sapiens Q02410 31413325
Intra
APP P05067 APBA1 Homo sapiens Q02410 8887653
Intra
APP P05067 PSMB8 Homo sapiens P28062-2 32814053
Intra
APP P05067 PSMB8 Homo sapiens P28062-2 32814053
Intra
APP P05067 PSMB8 Homo sapiens P28062-2 32814053
Intra
APP P05067 AATF Homo sapiens Q9NY61 32814053
Intra
APP P05067 AATF Homo sapiens Q9NY61 32814053
Intra
APP P05067 AATF Homo sapiens Q9NY61 32814053
Intra
APP P05067 TARDBP Homo sapiens Q13148 32814053
Intra
APP P05067 TARDBP Homo sapiens Q13148 32814053
Intra
APP P05067 TARDBP Homo sapiens Q13148 32814053
Intra
APP P05067 MAP1LC3B Homo sapiens Q9GZQ8 32814053
Intra
APP P05067 MAP1LC3B Homo sapiens Q9GZQ8 32814053
Intra
APP P05067 MAP1LC3B Homo sapiens Q9GZQ8 32814053
Intra
APP P05067 MPHOSPH6 Homo sapiens Q99547 32814053
Intra
APP P05067 MPHOSPH6 Homo sapiens Q99547 32814053
Intra
APP P05067 MPHOSPH6 Homo sapiens Q99547 32814053
Intra
APP P05067 SEPTIN5 Homo sapiens Q99719 32814053
Intra
APP P05067 SEPTIN5 Homo sapiens Q99719 32814053
Intra
APP P05067 SEPTIN5 Homo sapiens Q99719 32814053
Intra
APP P05067 VPS11 Homo sapiens Q9H270 32814053
Intra
APP P05067 VPS11 Homo sapiens Q9H270 32814053
Intra
APP P05067 VPS11 Homo sapiens Q9H270 32814053
Intra
APP P05067 HMGB1 Homo sapiens P09429 32814053
Intra
APP P05067 HMGB1 Homo sapiens P09429 32814053
Intra
APP P05067 HMGB1 Homo sapiens P09429 32814053
Intra
APP P05067 GTF2B Homo sapiens Q00403 32814053
Intra
APP P05067 GTF2B Homo sapiens Q00403 32814053
Intra
APP P05067 GTF2B Homo sapiens Q00403 32814053
Intra
APP P05067 GRK2 Homo sapiens P25098 32814053
Intra
APP P05067 GRK2 Homo sapiens P25098 32814053
Intra
APP P05067 GRK2 Homo sapiens P25098 32814053
Intra
APP P05067 PRKACG Homo sapiens P22612 32814053
Intra
APP P05067 PRKACG Homo sapiens P22612 32814053
Intra
APP P05067 PRKACG Homo sapiens P22612 32814053
Intra
APP P05067 MED12 Homo sapiens Q93074 21293490
Intra
APP P05067 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
APP P05067 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
APP P05067 RNF11 Homo sapiens Q9Y3C5 32814053
Intra
APP P05067 KAT5 Homo sapiens Q92993 32814053
Intra
APP P05067 KAT5 Homo sapiens Q92993 32814053
Intra
APP P05067 KAT5 Homo sapiens Q92993 32814053
Intra
APP P05067 UBB Homo sapiens P0CG47 32814053
Intra
APP P05067 UBB Homo sapiens P0CG47 32814053
Intra
APP P05067 UBB Homo sapiens P0CG47 32814053
Intra
APP P05067 RAC1 Homo sapiens P63000 32814053
Intra
APP P05067 RAC1 Homo sapiens P63000 32814053
Intra
APP P05067 RAC1 Homo sapiens P63000 32814053
Intra
APP P05067 PPIA Homo sapiens P62937 32814053
Intra
APP P05067 PPIA Homo sapiens P62937 32814053
Intra
APP P05067 PPIA Homo sapiens P62937 32814053
Intra
APP P05067 PPIA Homo sapiens P62937 16049941
Intra
APP P05067 CNTN2 Homo sapiens Q02246 32814053
Intra
APP P05067 CNTN2 Homo sapiens Q02246 32814053
Intra
APP P05067 CNTN2 Homo sapiens Q02246 32814053
Intra
APP P05067 MGARP Homo sapiens Q8TDB4 32814053
Intra
APP P05067 MGARP Homo sapiens Q8TDB4 32814053
Intra
APP P05067 MGARP Homo sapiens Q8TDB4 32814053
Intra
APP P05067 CDK1 Homo sapiens P06493 32814053
Intra
APP P05067 CDK1 Homo sapiens P06493 32814053
Intra
APP P05067 CDK1 Homo sapiens P06493 32814053
Intra
APP P05067 CYCS Homo sapiens P99999 32814053
Intra
APP P05067 CYCS Homo sapiens P99999 32814053
Intra
APP P05067 CYCS Homo sapiens P99999 32814053
Intra
APP P05067 RHOA Homo sapiens P61586 32814053
Intra
APP P05067 RHOA Homo sapiens P61586 32814053
Intra
APP P05067 RHOA Homo sapiens P61586 32814053
Intra
APP P05067 E2F1 Homo sapiens Q01094 32814053
Intra
APP P05067 E2F1 Homo sapiens Q01094 32814053
Intra
APP P05067 E2F1 Homo sapiens Q01094 32814053
Intra
APP P05067 HTT Homo sapiens P42858 32814053
Intra
APP P05067 HTT Homo sapiens P42858 32814053
Intra
APP P05067 HTT Homo sapiens P42858 32814053
Intra
APP P05067 PIAS4 Homo sapiens Q8N2W9 32814053
Intra
APP P05067 PIAS4 Homo sapiens Q8N2W9 32814053
Intra
APP P05067 PIAS4 Homo sapiens Q8N2W9 32814053
Intra
APP P05067 UTP14A Homo sapiens Q9BVJ6 32814053
Intra
APP P05067 UTP14A Homo sapiens Q9BVJ6 32814053
Intra
APP P05067 UTP14A Homo sapiens Q9BVJ6 32814053
Intra
APP P05067 PRKACA Homo sapiens P17612 32814053
Intra
APP P05067 PRKACA Homo sapiens P17612 32814053
Intra
APP P05067 PRKACA Homo sapiens P17612 32814053
Intra
APP P05067 PLK1 Homo sapiens P53350 32814053
Intra
APP P05067 PLK1 Homo sapiens P53350 32814053
Intra
APP P05067 PLK1 Homo sapiens P53350 32814053
Intra
APP P05067 TUBA1B Homo sapiens P68363 32814053
Intra
APP P05067 TUBA1B Homo sapiens P68363 32814053
Intra
APP P05067 TUBA1B Homo sapiens P68363 32814053
Intra
APP P05067 SPTB Homo sapiens P11277 32814053
Intra
APP P05067 SPTB Homo sapiens P11277 32814053
Intra
APP P05067 SPTB Homo sapiens P11277 32814053
Intra
APP P05067 FYN Homo sapiens P06241 32814053
Intra
APP P05067 FYN Homo sapiens P06241 32814053
Intra
APP P05067 FYN Homo sapiens P06241 32814053
Intra
APP P05067 CASP3 Homo sapiens P42574 32814053
Intra
APP P05067 CASP3 Homo sapiens P42574 32814053
Intra
APP P05067 CASP3 Homo sapiens P42574 32814053
Intra
APP P05067 ERP44 Homo sapiens Q9BS26 32814053
Intra
APP P05067 ERP44 Homo sapiens Q9BS26 32814053
Intra
APP P05067 ERP44 Homo sapiens Q9BS26 32814053
Intra
APP P05067 ARPP19 Homo sapiens P56211 32814053
Intra
APP P05067 ARPP19 Homo sapiens P56211 32814053
Intra
APP P05067 ARPP19 Homo sapiens P56211 32814053
Intra
APP P05067 PKN1 Homo sapiens Q16512 32814053
Intra
APP P05067 PKN1 Homo sapiens Q16512 32814053
Intra
APP P05067 PKN1 Homo sapiens Q16512 32814053
Intra
APP P05067 MAPK12 Homo sapiens P53778 32814053
Intra
APP P05067 MAPK12 Homo sapiens P53778 32814053
Intra
APP P05067 MAPK12 Homo sapiens P53778 32814053
Intra
APP P05067 CAV1 Homo sapiens Q03135 32814053
Intra
APP P05067 CAV1 Homo sapiens Q03135 32814053
Intra
APP P05067 CAV1 Homo sapiens Q03135 32814053
Intra
APP P05067 FLOT1 Homo sapiens O75955 16480949
Intra
APP P05067 FLOT1 Homo sapiens O75955 16480949
Intra
APP P05067 FLOT1 Homo sapiens O75955
Y2H
16480949
Intra
APP P05067 SSTR3 Homo sapiens P32745 32814053
Intra
APP P05067 SSTR3 Homo sapiens P32745 32814053
Intra
APP P05067 SSTR3 Homo sapiens P32745 32814053
Intra
APP P05067 RANBP9 Homo sapiens Q96S59 32814053
Intra
APP P05067 RANBP9 Homo sapiens Q96S59 32814053
Intra
APP P05067 RANBP9 Homo sapiens Q96S59 32814053
Intra
APP P05067 ICAM5 Homo sapiens Q9UMF0 32814053
Intra
APP P05067 ICAM5 Homo sapiens Q9UMF0 32814053
Intra
APP P05067 ICAM5 Homo sapiens Q9UMF0 32814053
Intra
APP P05067 PDGFRB Homo sapiens P09619 32814053
Intra
APP P05067 PDGFRB Homo sapiens P09619 32814053
Intra
APP P05067 PDGFRB Homo sapiens P09619 32814053
Intra
APP P05067 ARF3 Homo sapiens P61204 32814053
Intra
APP P05067 ARF3 Homo sapiens P61204 32814053
Intra
APP P05067 ARF3 Homo sapiens P61204 32814053
Intra
APP P05067 PPP2R5A Homo sapiens Q15172 32814053
Intra
APP P05067 PPP2R5A Homo sapiens Q15172 32814053
Intra
APP P05067 PPP2R5A Homo sapiens Q15172 32814053
Intra
APP P05067 GRK6 Homo sapiens P43250-2 32814053
Intra
APP P05067 GRK6 Homo sapiens P43250-2 32814053
Intra
APP P05067 GRK6 Homo sapiens P43250-2 32814053
Intra
APP P05067 BAD Homo sapiens Q92934 32814053
Intra
APP P05067 BAD Homo sapiens Q92934 32814053
Intra
APP P05067 BAD Homo sapiens Q92934 32814053
Intra
APP P05067 PDK1 Homo sapiens Q15118 32814053
Intra
APP P05067 PDK1 Homo sapiens Q15118 32814053
Intra
APP P05067 PDK1 Homo sapiens Q15118 32814053
Intra
APP P05067 APOA1 Homo sapiens P02647 11297421
Intra
APP P05067 APOA1 Homo sapiens P02647 11297421
Intra
APP P05067 ITGB1 Homo sapiens P05556 32814053
Intra
APP P05067 ITGB1 Homo sapiens P05556 32814053
Intra
APP P05067 ITGB1 Homo sapiens P05556 32814053
Intra
APP P05067 PRKCD Homo sapiens Q05655 32814053
Intra
APP P05067 PRKCD Homo sapiens Q05655 32814053
Intra
APP P05067 PRKCD Homo sapiens Q05655 32814053
Intra
APP P05067 PRKCE Homo sapiens Q02156 32814053
Intra
APP P05067 PRKCE Homo sapiens Q02156 32814053
Intra
APP P05067 PRKCE Homo sapiens Q02156 32814053
Intra
APP P05067 ZNF24 Homo sapiens P17028 32814053
Intra
APP P05067 ZNF24 Homo sapiens P17028 32814053
Intra
APP P05067 ZNF24 Homo sapiens P17028 32814053
Intra
APP P05067 CDKN2C Homo sapiens P42773 32814053
Intra
APP P05067 CDKN2C Homo sapiens P42773 32814053
Intra
APP P05067 CDKN2C Homo sapiens P42773 32814053
Intra
APP P05067 SAT1 Homo sapiens P21673 32814053
Intra
APP P05067 SAT1 Homo sapiens P21673 32814053
Intra
APP P05067 SAT1 Homo sapiens P21673 32814053
Intra
APP P05067 EIF2S2 Homo sapiens P20042 32814053
Intra
APP P05067 EIF2S2 Homo sapiens P20042 32814053
Intra
APP P05067 EIF2S2 Homo sapiens P20042 32814053
Intra
APP P05067 HMOX2 Homo sapiens P30519 32814053
Intra
APP P05067 HMOX2 Homo sapiens P30519 32814053
Intra
APP P05067 HMOX2 Homo sapiens P30519 32814053
Intra
APP P05067 NACA Homo sapiens Q13765 32814053
Intra
APP P05067 NACA Homo sapiens Q13765 32814053
Intra
APP P05067 NACA Homo sapiens Q13765 32814053
Intra
APP P05067 PNP Homo sapiens P00491 32814053
Intra
APP P05067 PNP Homo sapiens P00491 32814053
Intra
APP P05067 PNP Homo sapiens P00491 32814053
Intra
APP P05067 PPP2CA Homo sapiens P67775 32814053
Intra
APP P05067 PPP2CA Homo sapiens P67775 32814053
Intra
APP P05067 PPP2CA Homo sapiens P67775 32814053
Intra
APP P05067 TMSB4X Homo sapiens P62328 32814053
Intra
APP P05067 TMSB4X Homo sapiens P62328 32814053
Intra
APP P05067 TMSB4X Homo sapiens P62328 32814053
Intra
APP P05067 CHRNA4 Homo sapiens P43681 32814053
Intra
APP P05067 CHRNA4 Homo sapiens P43681 32814053
Intra
APP P05067 CHRNA4 Homo sapiens P43681 32814053
Intra
APP P05067 GSTM4 Homo sapiens Q03013 32814053
Intra
APP P05067 GSTM4 Homo sapiens Q03013 32814053
Intra
APP P05067 GSTM4 Homo sapiens Q03013 32814053
Intra
APP P05067 NDUFV2 Homo sapiens P19404 32814053
Intra
APP P05067 NDUFV2 Homo sapiens P19404 32814053
Intra
APP P05067 NDUFV2 Homo sapiens P19404 32814053
Intra
APP P05067 PIN1 Homo sapiens Q13526
LM
16554819
Intra
APP P05067 PIN1 Homo sapiens Q13526 32814053
Intra
APP P05067 PIN1 Homo sapiens Q13526 32814053
Intra
APP P05067 PIN1 Homo sapiens Q13526 32814053
Intra
APP P05067 TGIF1 Homo sapiens Q15583 32814053
Intra
APP P05067 TGIF1 Homo sapiens Q15583 32814053
Intra
APP P05067 TGIF1 Homo sapiens Q15583 32814053
Intra
APP P05067 UCHL1 Homo sapiens P09936 16049941
Intra
APP P05067 UCHL1 Homo sapiens P09936 32814053
Intra
APP P05067 UCHL1 Homo sapiens P09936 32814053
Intra
APP P05067 UCHL1 Homo sapiens P09936 32814053
Intra
APP P05067 COX5A Homo sapiens P20674 32814053
Intra
APP P05067 COX5A Homo sapiens P20674 32814053
Intra
APP P05067 COX5A Homo sapiens P20674 32814053
Intra
APP P05067 DCTN2 Homo sapiens Q13561 32814053
Intra
APP P05067 DCTN2 Homo sapiens Q13561 32814053
Intra
APP P05067 DCTN2 Homo sapiens Q13561 32814053
Intra
APP P05067 LRPAP1 Homo sapiens P30533 32814053
Intra
APP P05067 LRPAP1 Homo sapiens P30533 32814053
Intra
APP P05067 LRPAP1 Homo sapiens P30533 32814053
Intra
APP P05067 PDZK1IP1 Homo sapiens Q13113 32814053
Intra
APP P05067 PDZK1IP1 Homo sapiens Q13113 32814053
Intra
APP P05067 PDZK1IP1 Homo sapiens Q13113 32814053
Intra
APP P05067 PSAP Homo sapiens P07602 32814053
Intra
APP P05067 PSAP Homo sapiens P07602 32814053
Intra
APP P05067 PSAP Homo sapiens P07602 32814053
Intra
APP P05067 TOE1 Homo sapiens Q96GM8 32814053
Intra
APP P05067 TOE1 Homo sapiens Q96GM8 32814053
Intra
APP P05067 TOE1 Homo sapiens Q96GM8 32814053
Intra
APP P05067 UBA3 Homo sapiens Q8TBC4 32814053
Intra
APP P05067 UBA3 Homo sapiens Q8TBC4 32814053
Intra
APP P05067 UBA3 Homo sapiens Q8TBC4 32814053
Intra
APP P05067 PGAM1 Homo sapiens P18669 32814053
Intra
APP P05067 PGAM1 Homo sapiens P18669 16049941
Intra
APP P05067 PGAM1 Homo sapiens P18669 32814053
Intra
APP P05067 PGAM1 Homo sapiens P18669 32814053
Intra
APP P05067 BLMH Homo sapiens Q13867 32814053
Intra
APP P05067 BLMH Homo sapiens Q13867 32814053
Intra
APP P05067 BLMH Homo sapiens Q13867 32814053
Intra
APP P05067 NAE1 Homo sapiens Q13564 32814053
Intra
APP P05067 NAE1 Homo sapiens Q13564 32814053
Intra
APP P05067 NAE1 Homo sapiens Q13564 32814053
Intra
APP P05067 LINGO1 Homo sapiens Q96FE5 32814053
Intra
APP P05067 LINGO1 Homo sapiens Q96FE5 32814053
Intra
APP P05067 LINGO1 Homo sapiens Q96FE5 32814053
Intra
APP P05067 TRIM9 Homo sapiens Q9C026 32814053
Intra
APP P05067 TRIM9 Homo sapiens Q9C026 32814053
Intra
APP P05067 TRIM9 Homo sapiens Q9C026 32814053
Intra
APP P05067 GRK6 Homo sapiens P43250 32814053
Intra
APP P05067 GRK6 Homo sapiens P43250 32814053
Intra
APP P05067 GRK6 Homo sapiens P43250 32814053
Intra
APP P05067 SLC40A1 Homo sapiens Q9NP59 20817278
Intra
APP P05067 SLC40A1 Homo sapiens Q9NP59 24867889
Intra
APP P05067 ELK1 Homo sapiens P19419 32814053
Intra
APP P05067 ELK1 Homo sapiens P19419 32814053
Intra
APP P05067 ELK1 Homo sapiens P19419 32814053
Intra
APP P05067 SNCB Homo sapiens Q16143 32814053
Intra
APP P05067 SNCB Homo sapiens Q16143 32814053
Intra
APP P05067 SNCB Homo sapiens Q16143 32814053
Intra
APP P05067 CRYAB Homo sapiens P02511 16049941
Intra
APP P05067 HSPB2 Homo sapiens Q16082 32814053
Intra
APP P05067 HSPB2 Homo sapiens Q16082 32814053
Intra
APP P05067 HSPB2 Homo sapiens Q16082 32814053
Intra
APP P05067 DVL3 Homo sapiens Q92997 32814053
Intra
APP P05067 DVL3 Homo sapiens Q92997 32814053
Intra
APP P05067 DVL3 Homo sapiens Q92997 32814053
Intra
APP P05067 PCBD1 Homo sapiens P61457
TAP
20195357
Intra
APP P05067 RASD1 Homo sapiens Q9Y272 32814053
Intra
APP P05067 RASD1 Homo sapiens Q9Y272 32814053
Intra
APP P05067 RASD1 Homo sapiens Q9Y272 32814053
Intra
APP P05067 UBQLN1 Homo sapiens Q9UMX0 32814053
Intra
APP P05067 UBQLN1 Homo sapiens Q9UMX0 32814053
Intra
APP P05067 UBQLN1 Homo sapiens Q9UMX0 32814053
Intra
APP P05067 PAXIP1 Homo sapiens Q6ZW49 32814053
Intra
APP P05067 PAXIP1 Homo sapiens Q6ZW49 32814053
Intra
APP P05067 PAXIP1 Homo sapiens Q6ZW49 32814053
Intra
APP P05067 APPBP2 Homo sapiens Q92624 32814053
Intra
APP P05067 APPBP2 Homo sapiens Q92624 32814053
Intra
APP P05067 APPBP2 Homo sapiens Q92624 32814053
Intra
APP P05067 AIMP2 Homo sapiens Q13155 32814053
Intra
APP P05067 AIMP2 Homo sapiens Q13155 32814053
Intra
APP P05067 AIMP2 Homo sapiens Q13155 32814053
Intra
APP P05067 ZFC3H1 Homo sapiens O60293 35914814
Intra
APP P05067 ZFC3H1 Homo sapiens O60293 31413325
Intra
APP P05067 HOOK1 Homo sapiens Q9UJC3 32814053
Intra
APP P05067 HOOK1 Homo sapiens Q9UJC3 32814053
Intra
APP P05067 HOOK1 Homo sapiens Q9UJC3 32814053
Intra
APP P05067 DUSP6 Homo sapiens Q16828 32814053
Intra
APP P05067 DUSP6 Homo sapiens Q16828 32814053
Intra
APP P05067 DUSP6 Homo sapiens Q16828 32814053
Intra
APP P05067 NAA10 Homo sapiens P41227 32814053
Intra
APP P05067 NAA10 Homo sapiens P41227 32814053
Intra
APP P05067 NAA10 Homo sapiens P41227 32814053
Intra
APP P05067 PRPS1 Homo sapiens P60891 32814053
Intra
APP P05067 PRPS1 Homo sapiens P60891 32814053
Intra
APP P05067 PRPS1 Homo sapiens P60891 32814053
Intra
APP P05067 DR1 Homo sapiens Q01658 32814053
Intra
APP P05067 DR1 Homo sapiens Q01658 32814053
Intra
APP P05067 DR1 Homo sapiens Q01658 32814053
Intra
APP P05067 BSG Homo sapiens P35613 29423001
Intra
APP P05067 KCNIP3 Homo sapiens Q9Y2W7 32814053
Intra
APP P05067 KCNIP3 Homo sapiens Q9Y2W7 32814053
Intra
APP P05067 KCNIP3 Homo sapiens Q9Y2W7 32814053
Intra
APP P05067 CSNK1D Homo sapiens P48730 32814053
Intra
APP P05067 CSNK1D Homo sapiens P48730 32814053
Intra
APP P05067 CSNK1D Homo sapiens P48730 32814053
Intra
APP P05067 APP Homo sapiens P05067
EM
16286452
Intra
APP P05067 APP Homo sapiens P05067 20573181
Intra
APP P05067 APP Homo sapiens P05067 19549187
Intra
APP P05067 APP Homo sapiens P05067 18805418
Intra
APP P05067 APP Homo sapiens P05067 19754881
Intra
APP P05067 APP Homo sapiens P05067
CD
18805418
Intra
APP P05067 APP Homo sapiens P05067
CD
19549187
Intra
APP P05067 APP Homo sapiens P05067
AFM
20818335
Intra
APP P05067 APP Homo sapiens P05067
NMR
19549187
Intra
APP P05067 APP Homo sapiens P05067 19549187
Intra
APP P05067 APP Homo sapiens P05067
AFM
19549187
Intra
APP P05067 APP Homo sapiens P05067 20818335
Intra
APP P05067 APP Homo sapiens P05067 20818335
Intra
APP P05067 APP Homo sapiens P05067 18805418
Intra
APP P05067 TP53BP2 Homo sapiens Q13625 11278849
Intra
APP P05067 TP53BP2 Homo sapiens Q13625 11278849
Intra
APP P05067 BCAP31 Homo sapiens P51572 32814053
Intra
APP P05067 BCAP31 Homo sapiens P51572 32814053
Intra
APP P05067 BCAP31 Homo sapiens P51572 32814053
Intra
APP P05067 BCL2 Homo sapiens P10415 32814053
Intra
APP P05067 BCL2 Homo sapiens P10415 32814053
Intra
APP P05067 BCL2 Homo sapiens P10415 32814053
Intra
APP P05067 TGFB2 Homo sapiens P61812 2119582
Intra
APP P05067 TGFB1 Homo sapiens P01137
PLA
25241761
Intra
APP P05067 TGFB1 Homo sapiens P01137 2119582
Intra
APP P05067 CASP8 Homo sapiens Q14790 32814053
Intra
APP P05067 CASP8 Homo sapiens Q14790 32814053
Intra
APP P05067 CASP8 Homo sapiens Q14790 32814053
Intra
APP P05067 CBX1 Homo sapiens P83916 32814053
Intra
APP P05067 CBX1 Homo sapiens P83916 32814053
Intra
APP P05067 CBX1 Homo sapiens P83916 32814053
Intra
APP P05067 SYK Homo sapiens P43405 32814053
Intra
APP P05067 SYK Homo sapiens P43405 32814053
Intra
APP P05067 SYK Homo sapiens P43405 32814053
Intra
APP P05067 MAPK8IP1 Homo sapiens Q9UQF2 35914814
Intra
APP P05067 MAPK8IP1 Homo sapiens Q9UQF2 31413325
Intra
APP P05067 MAPK8IP1 Homo sapiens Q9UQF2 11724784
Intra
APP P05067 SCARB1 Homo sapiens Q8WTV0 32814053
Intra
APP P05067 SCARB1 Homo sapiens Q8WTV0 32814053
Intra
APP P05067 SCARB1 Homo sapiens Q8WTV0 32814053
Intra
APP P05067 SHC1 Homo sapiens P29353 11877420
Intra
APP P05067 SHC3 Homo sapiens Q92529 32814053
Intra
APP P05067 SHC3 Homo sapiens Q92529 32814053
Intra
APP P05067 SHC3 Homo sapiens Q92529 32814053
Intra
APP P05067 APBB2 Homo sapiens Q92870 35914814
Intra
APP P05067 APBB2 Homo sapiens Q92870 31413325
Intra
APP P05067 CHRNA7 Homo sapiens P36544 32814053
Intra
APP P05067 CHRNA7 Homo sapiens P36544 32814053
Intra
APP P05067 CHRNA7 Homo sapiens P36544 32814053
Intra
APP P05067 LYN Homo sapiens P07948 32814053
Intra
APP P05067 LYN Homo sapiens P07948 32814053
Intra
APP P05067 LYN Homo sapiens P07948 32814053
Intra
APP P05067 NOTCH4 Homo sapiens Q99466 32814053
Intra
APP P05067 NOTCH4 Homo sapiens Q99466 32814053
Intra
APP P05067 NOTCH4 Homo sapiens Q99466 32814053
Intra
APP P05067 HSD17B10 Homo sapiens Q99714 32814053
Intra
APP P05067 HSD17B10 Homo sapiens Q99714 32814053
Intra
APP P05067 HSD17B10 Homo sapiens Q99714 9338779
Intra
APP P05067 HSD17B10 Homo sapiens Q99714 32814053
Intra
APP P05067 PABPC1 Homo sapiens P11940 32814053
Intra
APP P05067 PABPC1 Homo sapiens P11940 32814053
Intra
APP P05067 PABPC1 Homo sapiens P11940 32814053
Intra
APP P05067 APBB1 Homo sapiens O00213 16049941
Intra
APP P05067 APBB1 Homo sapiens O00213 31413325
Intra
APP P05067 APBB1 Homo sapiens O00213
Y2H
9461550
Intra
APP P05067 APBB1 Homo sapiens O00213 35914814
Cross
APP P05067 q306t3_9actn Streptomyces sp. KK565 Q306T3 20828565
Intra
APP P05067 JUN Homo sapiens P05412 20195357
Intra
APP P05067 JUN Homo sapiens P05412 32814053
Intra
APP P05067 JUN Homo sapiens P05412 32814053
Intra
APP P05067 JUN Homo sapiens P05412 32814053
Intra
APP P05067 FOS Homo sapiens P01100
TAP
20195357
Intra
APP P05067 ADCYAP1 Homo sapiens P18509 32814053
Intra
APP P05067 ADCYAP1 Homo sapiens P18509 32814053
Intra
APP P05067 ADCYAP1 Homo sapiens P18509 32814053
Intra
APP P05067 DRD4 Homo sapiens P21917 32814053
Intra
APP P05067 DRD4 Homo sapiens P21917 32814053
Intra
APP P05067 DRD4 Homo sapiens P21917 32814053
Intra
APP P05067 RAB6A Homo sapiens P20340-2 32814053
Intra
APP P05067 RAB6A Homo sapiens P20340-2 32814053
Intra
APP P05067 RAB6A Homo sapiens P20340-2 32814053
Intra
APP P05067 SYP Homo sapiens P08247 32814053
Intra
APP P05067 SYP Homo sapiens P08247 32814053
Intra
APP P05067 SYP Homo sapiens P08247 32814053
Intra
APP P05067 ACAN Homo sapiens P16112 32814053
Intra
APP P05067 ACAN Homo sapiens P16112 32814053
Intra
APP P05067 ACAN Homo sapiens P16112 32814053
Intra
APP P05067 CSNK1D Homo sapiens P48730-2 32814053
Intra
APP P05067 CSNK1D Homo sapiens P48730-2 32814053
Intra
APP P05067 CSNK1D Homo sapiens P48730-2 32814053
Intra
APP P05067 PIK3R1 Homo sapiens P27986-2 32814053
Intra
APP P05067 PIK3R1 Homo sapiens P27986-2 32814053
Intra
APP P05067 PIK3R1 Homo sapiens P27986-2 32814053
Intra
APP P05067 ATXN1 Homo sapiens P54253 32814053
Intra
APP P05067 ATXN1 Homo sapiens P54253 32814053
Intra
APP P05067 ATXN1 Homo sapiens P54253 32814053
Intra
APP P05067 CTCF Homo sapiens P49711 32814053
Intra
APP P05067 CTCF Homo sapiens P49711 32814053
Intra
APP P05067 CTCF Homo sapiens P49711 32814053
Intra
APP P05067 KCNAB2 Homo sapiens Q13303 32814053
Intra
APP P05067 KCNAB2 Homo sapiens Q13303 32814053
Intra
APP P05067 KCNAB2 Homo sapiens Q13303 32814053
Intra
APP P05067 SNX6 Homo sapiens Q9UNH7 32814053
Intra
APP P05067 SNX6 Homo sapiens Q9UNH7 32814053
Intra
APP P05067 SNX6 Homo sapiens Q9UNH7 32814053
Intra
APP P05067 MAPK1 Homo sapiens P28482 32814053
Intra
APP P05067 MAPK1 Homo sapiens P28482 32814053
Intra
APP P05067 MAPK1 Homo sapiens P28482 32814053
Intra
APP P05067 STXBP1 Homo sapiens P61764 16049941
Intra
APP P05067 STXBP1 Homo sapiens P61764 32814053
Intra
APP P05067 STXBP1 Homo sapiens P61764 32814053
Intra
APP P05067 STXBP1 Homo sapiens P61764 32814053
Intra
APP P05067 FLNA Homo sapiens P21333-2 32814053
Intra
APP P05067 FLNA Homo sapiens P21333-2 32814053
Intra
APP P05067 FLNA Homo sapiens P21333-2 32814053
Intra
APP P05067 MAT1A Homo sapiens Q00266 32814053
Intra
APP P05067 MAT1A Homo sapiens Q00266 32814053
Intra
APP P05067 MAT1A Homo sapiens Q00266 32814053
Intra
APP P05067 MARK1 Homo sapiens Q9P0L2 32814053
Intra
APP P05067 MARK1 Homo sapiens Q9P0L2 32814053
Intra
APP P05067 MARK1 Homo sapiens Q9P0L2 32814053
Intra
APP P05067 PDIA3 Homo sapiens P30101 15896298
Intra
APP P05067 PDIA3 Homo sapiens P30101 15896298
Intra
APP P05067 PDIA3 Homo sapiens P30101 32814053
Intra
APP P05067 PDIA3 Homo sapiens P30101 32814053
Intra
APP P05067 PDIA3 Homo sapiens P30101 32814053
Intra
APP P05067 SNCA Homo sapiens P37840 32814053
Intra
APP P05067 SNCA Homo sapiens P37840 32814053
Intra
APP P05067 SNCA Homo sapiens P37840 32814053
Intra
APP P05067 SNCA Homo sapiens P37840
PLA
25241761
Intra
APP P05067 SLC36A1 Homo sapiens Q7Z2H8 32814053
Intra
APP P05067 SLC36A1 Homo sapiens Q7Z2H8 32814053
Intra
APP P05067 SLC36A1 Homo sapiens Q7Z2H8 32814053
Intra
APP P05067 TMED10 Homo sapiens P49755 32814053
Intra
APP P05067 TMED10 Homo sapiens P49755 32814053
Intra
APP P05067 TMED10 Homo sapiens P49755 32814053
Intra
APP P05067 PSENEN Homo sapiens Q9NZ42 32814053
Intra
APP P05067 PSENEN Homo sapiens Q9NZ42 32814053
Intra
APP P05067 PSENEN Homo sapiens Q9NZ42 32814053
Intra
APP P05067 GRIN1 Homo sapiens Q05586 32814053
Intra
APP P05067 GRIN1 Homo sapiens Q05586 32814053
Intra
APP P05067 GRIN1 Homo sapiens Q05586 32814053
Cross
APP P05067 Apba2 Rattus norvegicus O35431 22730553
Cross
APP P05067 Apba2 Rattus norvegicus O35431 22730553
Cross
APP P05067 CALR Oryctolagus cuniculus P15253 23585889
Cross
APP P05067 CALR Oryctolagus cuniculus P15253 23585889
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant APP Proteins

Cat. No. Nom du produit Accession Pureté
HY-P7501 Amyloid Precursor/APP-695 Protein, Human (HEK293, Fc) P05067-4 (L18-K612) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P72834 Amyloid Precursor/APP-751 Protein, Human (HEK293, Fc) P05067-8/NP_958816.1 (L18-L669) ≥ 95%, as determined by reducing SDS-PAGE.
HY-P75511 Amyloid Precursor/Beta-APP40 Protein, Human (His-GST) P05067-1 (D672-V711) ≥ 90%, as determined by reducing SDS-PAGE.
HY-P76168 Amyloid Precursor/Beta-APP42 Protein, Human (His-GST) P05067-1 (D672-A713) ≥ 95%, as determined by reducing SDS-PAGE.

APP Anticorps

Cat. No. Nom du produit Application Reactivity
HY-P81385 Amyloid Precursor Protein Antibody (YA1130) IHC-P Human
HY-P81385A Amyloid Precursor Protein Antibody (YA1130)(PBS only) IHC-P Human
HY-P82823 Phospho-Amyloid Precursor Protein (Thr743) Antibody (YA2568) WB, ICC/IF, IP Human, Rat
HY-P82823A Phospho-Amyloid Precursor Protein (Thr743) Antibody (YA2568)(PBS only) WB, ICC/IF, IP Human, Rat
HY-P83753 beta Amyloid 1-40 Antibody (YA3554) WB, IHC-P, IF-Tissue Human, Mouse
HY-P83753A beta Amyloid 1-40 Antibody (YA3554)(PBS only) WB, IHC-P, IF-Tissue Human, Mouse
HY-P83754 beta Amyloid 1-42 Antibody (YA3555) WB, IHC-P, IF-Tissue Human, Mouse
HY-P83754A beta Amyloid 1-42 Antibody (YA3555)(PBS only) WB, IHC-P, IF-Tissue Human, Mouse
HY-P83755 beta Amyloid Antibody (YA3556) WB, IHC-P, ICC/IF, Dot Blot Human, Mouse
HY-P83755A beta Amyloid Antibody (YA3556)(PBS only) WB, IHC-P, IF-Tissue, Dot Blot Human, Mouse
HY-P86422 beta-Amyloid Antibody (YA6114) WB, IHC-P, ICC/IF, IP, ELISA Human, Mouse, Rat
HY-P86747 beta-Amyloid 1-42 Antibody (YA6439) WB, IHC-P, IHC-F, IF-Tissue Human
HY-P86747A beta-Amyloid 1-42 Antibody (YA6439)(PBS only) WB, IHC-P, IHC-F, IF-Tissue Human

Related Diseases

Diseases Alias
Schizophrenia
  • SCZD

  • Schizophrenia With Or Without An Affective Disorder

  • Schizophrenia 12

  • Schizophrenia, Susceptibility To

  • Schizophrenia-1

  • Dementia Praecox

  • Schizophrenia 1

Myositis
  • Idiopathic Inflammatory Myopathy

  • Idiopathic Inflammatory Myositis

  • Iim

  • Imm

  • Idiopathic Inflammatory Myopathies

  • Myopathy, Familial Idiopathic Inflammatory

  • Inflammatory Disorder Of Muscle

  • Idiopathic Inflammatory Myopathy, Familial

  • Inflammatory Myopathy, Idiopathic

  • Myopathies Idiopathic Inflammatory

  • Familial Idiopathic Inflammatory Myopathy

Alzheimer'S Disease 1
  • Alzheimer Disease Type 1

  • Alzheimer'S Disease 1, Early Onset

Chromosomal Duplication Syndrome
Normal Pressure Hydrocephalus
  • Low Pressure Hydrocephalus

  • Hydrocephalus Normal Pressure

  • Hydrocephalus, Normal Pressure

  • Normal Pressure Hydrocephalus Nos

  • Nph - [Normal Pressure Hydrocephalus]

  • Normal Pressure Hydrocephaly

Motor Neuron Disease
  • Anterior Horn Cell Disease

  • Motor Neuron Diseases

  • Mnd - [Motor Neurone Disease]

  • Lou Gehrig Disease

  • Creeping Palsy

  • Creeping Paralysis

  • Bulbar Motor Neuron Disease

  • Bulbar Syndrome

  • Anterior Horn Cell Disorder

  • Hereditary Motor Neuron Disease

Senile Plaque Formation
Senile Degeneration Of Brain
  • Senile Brain Degen.

Cerebral Atherosclerosis
  • Intracranial Arteriosclerosis

Huntington Disease
  • Huntington'S Disease

  • Huntington Chorea

  • HD

  • Huntington'S Chorea

  • Huntington Chronic Progressive Hereditary Chorea

  • Juvenile Huntington Disease

  • Chronic Progressive Chorea

  • Chronic Progressive Hereditary Chorea

  • Hc - [Huntington Chorea]

  • Hereditary Chorea

  • Progressive Hereditary Chorea

Cerebral Amyloid Angiopathy, Cst3-Related
  • Cerebral Amyloid Angiopathy

  • Hereditary Cerebral Hemorrhage With Amyloidosis

  • Hchwa

  • Cerebral Amyloid Angiopathy, Familial

  • Hereditary Cystatin C Amyloid Angiopathy

  • Amyloidosis, Cerebroarterial, Icelandic Type

  • Amyloidosis Vi

  • Cerebral Hemorrhage, Hereditary, With Amyloidosis

  • Cst3-Related Cerebral Amyloid Angiopathy

  • Cerebral Hemorrhage, Hereditary, With Amyloidosis, Icelandic Variant

  • Hereditary Cerebral Hemorrhage With Amyloidosis, Icelandic Variant

  • Caa, Familial

  • Cerebral Amyloid Angiopathy, Genetic

  • Acys Amyloidosis

  • Cst3-Related Amyloidosis

  • Cystatin Amyloidosis

  • Hchwa, Icelandic Type

  • Hereditary Cerebral Hemorrhage With Amyloidosis, Icelandic Type

  • Amyloidosis 6

  • AMYL6

  • Acys

  • Caa

  • Cerebral Amyloid Angiopathy Cst3-Related

  • Cerebroarterial Amyloidosis Icelandic Type

  • Cystatin C Amyloidosis

  • Hccaa

  • Hchwai

  • Hchwa-I

  • Hereditary Cerebral Hemorrhage With Amyloidosis Icelandic Type

  • Cerebral Amyloid Angiopathy Familial

  • Angiopathy, Amyloid, Cerebral, Cst3-Related

  • Hereditary Cerebral Amyloid Angiopathy, Icelandic Type

  • Familial Cerebral Amyloid Angiopathy

  • Cerebral Amyloid Angiopathy, Hereditary

Prion Disease
  • Spongiform Encephalopathy

  • Transmissible Spongiform Encephalopathies

  • Prion Diseases

  • Prion Disease Pathway

  • Transmissible Spongiform Encephalopathy

  • Prion Induced Disorder

  • Prion Protein Disease

  • Inherited Human Transmissible Spongiform Encephalopathies

  • Prion Protein Diseases

  • Prion-Associated Disorders

  • Prion-Induced Disorders

  • Transmissible Dementias

  • Tses

  • Human Prion Disease

  • Tse

  • Encephalopathy, Transmissible Spongiform

  • Prion Disease, Susceptibility To

  • Spongiform Encephalopathies

  • Human Transmissible Spongiform Encephalopathies, Inherited

Alzheimer Disease 3
  • AD3

  • Alzheimer Disease, Type 3

  • Alzheimer Disease, Type 3, With Spastic Paraparesis And Unusual Plaques

  • Alzheimer Disease, Type 3, With Spastic Paraparesis And Apraxia

  • Alzheimer'S Disease 3

  • Alzheimer Disease, Familial, 3, With Spastic Paraparesis And Apraxia

  • Alzheimer Disease 3, Early-Onset

  • Alzheimer Disease, Familial, 3

  • Alzheimer Disease, Protection Against, Due To Apoe3-Christchurch

  • Alzheimer Disease 3, Early Onset

  • Alzheimer Disease Familial 3

  • Early-Onset Familial Alzheimer Disease 3

  • Familial Alzheimer Disease 3

  • Familial Alzheimer Disease 3 With Spastic Paraparesis And Apraxia

  • Familial Alzheimer Disease 3 With Spastic Paraparesis And Unusual Plaques

  • Alzheimer Disease, Familial, 3, With Spastic Paraparesis And Unusual Plaques

  • Alzheimer Disease, Familial, Type 3

Alzheimer Disease 2
  • AD2

  • Alzheimer Disease Associated With Apoe4

  • Alzheimer'S Disease 2

  • Alzheimer Disease-2

  • Alzheimer Disease 2, Late-Onset

  • Alzheimer Disease 2, Late Onset

  • Late-Onset Alzheimer Disease

  • Alzheimer Disease, Type 2

  • Alzheimer Disease, Late Onset

Chronic Wasting Disease
  • Wasting Disease, Chronic

Hydrocephalus
  • Hydrocephalus, Nonsyndromic, Autosomal Recessive

  • Hydrocephalus, X-Linked

  • Hydrocephalus Adverse Event

  • Hydrocephaly Nos

Tangier Disease
  • Analphalipoproteinemia

  • High Density Lipoprotein Deficiency, Tangier Type

  • TGD

  • High Density Lipoprotein Deficiency, Type 1

  • Hdldt1

  • Familial High Density Lipoprotein Deficiency

  • A-Alphalipoprotein Neuropathy

  • Alpha High Density Lipoprotein Deficiency Disease

  • Cholesterol Thesaurismosis

  • Familial High Density Lipoprotein Deficiency Disease

  • Hdl Lipoprotein Deficiency Disease

  • Tangier Disease Neuropathy

  • Familial Alpha-Lipoprotein Deficiency

  • Familial High-Density Lipoprotein Deficiency 1

  • Primary Hypoalphalipoproteinemia 1

  • Analphalipo-Proteinemia

  • Familial Hypoalphalipo-Proteinemia

  • Familial Hypoalphalipoproteinemia

  • Lipoprotein Deficiency Disease, Hdl, Familial

  • Tangier Hereditary Neuropathy

  • Atp-Binding Cassette Transporter A1 Deficiency

  • Hdld1

  • High Density Lipoprotein Deficiency 1

  • Tangier Disease, Variant

  • Hypoalphalipoproteinemia, Familial

  • Familial Hdl Deficiency

Cerebral Amyloid Angiopathy, Itm2b-Related, 1
  • Dementia, Familial British

  • Fbd

  • Presenile Dementia With Spastic Ataxia

  • Familial British Dementia

  • Abri Amyloidosis

  • Cerebral Amyloid Angiopathy, British Type

  • Itm2b-Related Cerebral Amyloid Angiopathy 1

  • Familial Dementia, British Type

  • Cerebral Amyloid Angiopathy, Itm2b-Related 1

  • CAA-ITM2B1

  • Cerebral Amyloid Angiopathy British Type

  • Dementia, Familial, British

Cutaneous Ganglioneuroma
  • Ganglioneuroma Of Skin

Dementia, Lewy Body
  • Lewy Body Dementia

  • Lewy Body Disease

  • Diffuse Lewy Body Disease

  • Dementia With Lewy Bodies

  • DLB

  • Autosomal Dominant Diffuse Lewy Body Disease

  • Cortical Lewy Body Disease

  • Dementia, Lewy Body, Susceptibility To

  • Lewy Body Dementia, Susceptibility To

  • Senile Dementia Of The Lewy Body Type

  • Dementia Of The Lewy Body Type

  • Lbd

  • Diffuse Lewy Body Disease With Gaze Palsy

  • Dysphasic Dementia Hereditary

  • Lewy Body Type Senile Dementia

  • Lewy Body Variant Of Alzheimer Disease

  • Lewy Bodies

  • Lewy Body

  • Dlbd - [Diffuse Lewy Body Disease]

  • Clbd - [Cortical Lewy Body Disease]

Specific Developmental Disorder
Inclusion Body Myositis
  • Ibm

  • Sporadic Inclusion Body Myositis

  • Myositis, Inclusion Body

  • Inflammatory Myopathy

  • Inflammatory Myopathies

  • Sibm

  • Myositis Inclusion Body

  • Nonaka Myopathy

  • Inclusion Body Myopathy, Autosomal Recessive

  • Inclusion Body Myopathy, Autosomal Dominant

  • Myositis

  • Inclusion Body Myopathy, Sporadic

Cerebellar Disease
  • Cerebellar Diseases

  • Cerebellar Dysfunction

  • Cerebellar Abnormality

  • Cerebellar Disorders

Lesch-Nyhan Syndrome
  • Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency

  • LNS

  • Hprt Deficiency

  • Complete Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency

  • Hypoxanthine Guanine Phosphoribosyltransferase Deficiency

  • X-Linked Hyperuricemia

  • Choreoathetosis Self-Mutilation Syndrome

  • Hprt1 Deficiency

  • Hprt Deficiency, Complete

  • Deficiency Of Imp Pyrophosphorylase

  • Hgprt Deficiency

  • Lesch-Nyhan Disease

  • Hypoxanthine Guanine Phosphoribosyltransferase 1 Deficiency

  • Hg-Prt Deficiency

  • Hypoxanthine-Guanine-Phosphoribosyltransferase Deficiency

  • Lesch - Nyhan Syndrome

  • Hprt1 Disorders

  • Lesch Nyhan Syndrome

  • Complete Hprt Deficiency Complete

  • Lesch Nyhan Disease

  • Complete Hprt Deficiency

  • Deficiency Of Guanine Phosphoribosyltransferase

  • Deficiency Of Hypoxanthine Phosphoribosyltransferase

  • Hypoxanthine Phosphoribosyltransferase Deficiency

  • Juvenile Gout, Choreoathetosis, Mental Retardation Syndrome

  • Juvenile Hyperuricemia Syndrome

  • Lnd

  • Primary Hyperuricemia Syndrome

  • Total Hprt Deficiency

  • Total Hypoxanthine-Guanine Phosphoribosyl Transferase Deficiency

  • X-Linked Primary Hyperuricemia

  • X-Linked Uric Aciduria Enzyme Defect

  • Hprt Complete Deficiency

  • Hprt Deficiency Grade Iv

  • Hypoxanthine Guanine Phosphoribosyltransferase Complete Deficiency

  • Hypoxanthine Guanine Phosphoribosyltransferase Deficiency, Grade Iv

  • Hypoxanthine-Guanine Phosphoribosyltransferase 1 Deficiency

  • Hprt - [ Hypoxanthine-Guanine Phosphoribosyltransferase] Complete Deficiency

  • Total Hgprt - [Hypoxanthine-Guanine Phosphoribosyltransferase] Deficiency

Amyloidosis
  • Amyloid Disease

  • Amyloid

  • Amyloid Degeneration

  • Amyloidosis Nos

  • Amyloid Deposition

  • Amyloid Infiltration

  • Idiopathic Amyloidosis

  • Hyaloid Degeneration

  • Lardaceous Degeneration

Communicating Hydrocephalus
  • Acquired Communicating Hydrocephalus

Meningoencephalitis
  • Acquired Toxoplasmal Meningoencephalitis

  • Meningoencephalitis Due To Acquired Toxoplasmosis

  • Meningoencephalitis Due To Toxoplasmosis

  • Toxoplasma Meningoencephalitis

Ovarian Cancer
  • Ovarian Carcinoma

  • Ovarian Neoplasm

  • Malignant Tumour Of Ovary

  • Epithelial Ovarian Cancer

  • Neoplasm Of Ovary

  • Ovarian Neoplasms

  • Ovarian Cancers

  • Malignant Neoplasm Of Ovary

  • Primary Malignant Neoplasm Of Ovary

  • Ovarian Cancer, Somatic

  • Malignant Ovarian Tumor

  • Ovary Neoplasm

  • Primary Ovarian Cancer

  • Tumor Of The Ovary

  • Cancer Of The Ovary

  • Malignant Neoplasm Of The Ovary

  • Malignant Tumor Of The Ovary

  • Ovarian Malignant Tumor

  • OC

  • Ovarian Carcinomas

  • Cancer, Ovarian

  • Cancer Of Ovary

  • Ovary Cancer

  • Ca Ovary

Neurodegeneration With Brain Iron Accumulation 2a
  • Infantile Neuroaxonal Dystrophy

  • Plan

  • Seitelberger Disease

  • Inad

  • Infantile Neuroaxonal Dystrophy 1

  • Inad1

  • Pla2g6-Associated Neurodegeneration

  • NBIA2A

  • Neuroaxonal Dystrophy, Infantile

  • Neurodegeneration, Pla2g6-Associated

  • Neurodegeneration With Brain Iron Accumulation, Pla2g6-Related

  • Phospholipase A2-Associated Neurodegeneration

  • Nbia2

  • Pla2g6-Related Disorders

  • Infantile Neuroaxonal Dystrophy/Atypical Neuroaxonal Dystrophy

  • Karak Syndrome, Included

  • Nbia2b

  • Neuroaxonal Dystrophy, Atypical

  • Neurodegeneration With Brain Iron Accumulation 2b

  • Nbia, Pla2g6-Related

  • Seitelberger'S Disease

  • Neurodegeneration Pla2g6-Associated

  • Dystrophy, Neuroaxonal, Infantile

  • Neurodegeneration, With Brain Iron Accumulation, Type 2a

  • Neuroaxonal Dystrophies

  • Neurodegeneration With Brain Iron Accumulation 2

Hereditary Spastic Paraplegia
  • Familial Spastic Paraplegia

  • Hereditary Spastic Paraparesis

  • Strumpell-Lorrain Disease

  • Hsp

  • Spg

  • Strümpell-Lorrain Disease

  • Spastic Paraplegia, Hereditary

  • French Settlement Disease

  • Strumpell-Lorrain Syndrome

  • Fsp

  • Familial Spastic Paraparesis

  • Spastic Paraplegia, Familial

  • Spastic Paraplegia Hereditary

  • Spastic Paraplegia 3, Autosomal Dominant

  • Spastic Paraparesis

  • Hereditary Spastic Paralysis

  • Familial Spastic Paralysis

  • Hereditary Spastic Ataxia

Abcd Syndrome
  • ABCDS

  • Albinism, Black Lock, Cell Migration Disorder Of The Neurocytes Of The Gut, And Deafness

  • Albinism, Black Lock, Cell Migration Disorder Of The Neurocytes Of The Gut And Deafness

Myopathy
  • Muscular Diseases

  • Myopathies

Cerebral Degeneration
  • Brain Degeneration

  • Degenerative Brain Disorder

Macular Degeneration, Age-Related, 1
  • Macular Degeneration

  • Age-Related Macular Degeneration

  • Macular Degeneration, Age-Related

  • Age Related Macular Degeneration

  • Age Related Macular Degeneration 1

  • ARMD1

  • Maculopathy, Age-Related, 1

  • Macular Degeneration, Age-Related, Reduced Risk Of

  • Age Related Maculopathy 1

  • Age Related Maculopathies

  • Age Related Maculopathy

  • Senile Macular Degeneration

  • Senile Macular Retinal Degeneration

  • Macular Degeneration Of Retina

  • Age-Related Maculopathy

  • Amd

  • Armd

  • Age-Related Maculopathy, Susceptibility To

  • Maculopathy Age-Related

  • Macular Degeneration, Age-Related, 1, Susceptibility To

  • Maculopathy, Age-Related

  • Macular Degeneration, Age-Related, Type 1

  • Macular Degeneration, Age-Related, 2

Charcot-Marie-Tooth Disease
  • Cmt

  • Hmsn

  • Hereditary Motor And Sensory Neuropathy

  • Pma

  • Cmt - Charcot-Marie-Tooth Disease

  • Charcot Marie Tooth Disease

  • Charcot-Marie-Tooth Hereditary Neuropathy

  • Charcot-Marie-Tooth Syndrome

  • Peroneal Muscular Atrophy

  • Hereditary Motor And Sensory Neuropathies

Early-Onset, Autosomal Dominant Alzheimer Disease
  • Familial Alzheimer Disease

  • Early-Onset Autosomal Dominant Alzheimer Disease

  • Eofad

  • Early-Onset Familial Autosomal Dominant Alzheimer Disease

  • Alzheimer'S Disease, Familial

Periventricular Leukomalacia
  • Leukomalacia, Periventricular

  • Pvl

  • Leukomalacia Periventricular

Frontotemporal Dementia
  • Pallidopontonigral Degeneration

  • Frontotemporal Lobar Degeneration

  • Semantic Dementia

  • FTD

  • Frontotemporal Lobe Dementia

  • Multiple System Tauopathy With Presenile Dementia

  • Dementia, Frontotemporal

  • Frontotemporal Dementia With Parkinsonism

  • Mstd

  • Frontotemporal Lobar Degeneration With Tau Inclusions

  • Ftld With Tau Inclusions

  • Dementia, Frontotemporal, With Parkinsonism

  • Fldem

  • Ftdp17

  • Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex

  • Ddpac

  • Wilhelmsen-Lynch Disease

  • Wld

  • Ppnd

  • Dementia, Frontotemporal, With Or Without Parkinsonism

  • Semantic Primary Progressive Aphasia

  • Semantic Variant Ppa

  • Wilhemsen-Lynch Disease

  • Frontotemporal Dementia-Amyotrophic Lateral Sclerosis

  • Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17

  • Ftd-Als

  • Ftld

  • Pick Complex

  • Pick Disease Of The Brain

  • Frontotemporal Dementia With Parkinsonism-17

  • Grn-Related Frontotemporal Dementia

  • Frontotemporal Dementia With Motor Neuron Disease

  • Dementia In Fronto-Temporal Lobar Degeneration

  • Ftd - [Frontotemporal Dementia]

  • Temple Dementia

  • Frontal Lobe Dementia

Gerstmann-Straussler Disease
  • Gerstmann-Straussler-Scheinker Disease

  • Gerstmann-Straussler-Scheinker Syndrome

  • Prion Dementia

  • Cerebral Amyloid Angiopathy, Prnp-Related

  • GSD

  • Gss

  • Cerebellar Ataxia, Progressive Dementia, And Amyloid Deposits In Cns

  • Amyloidosis, Cerebral, With Spongiform Encephalopathy

  • Subacute Spongiform Encephalopathy, Gerstmann-Straussler Type

  • Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type

  • Amyloidosis Cerebral With Spongiform Encephalopathy

  • Cerebellar Ataxia, Progressive Dementia, And Amyloid Deposits In The Central Nervous System

  • Encephalopathy Subacute Spongiform Gerstmann-Straussler Type

  • Gssd

  • Gerstmann Straussler Scheinker Syndrome

  • Cerebral Amyloidosis With Spongiform Encephalopathy

  • Subacute Spongiform Encephalopathy Gerstmann-Straussler Type

  • Gluthathione Synthetase Deficiency

  • Gerstmann Straussler Syndrome

Neuronal Ceroid Lipofuscinosis
  • Hereditary Ceroid Lipofuscinosis

  • Batten Disease

  • Ncl

  • Neuronal Ceroid-Lipofuscinoses

  • Lipofuscinosis, Ceroid, Neuronal

  • Juvenile Neuronal Ceroid Lipofuscinosis

  • Cerebromacular Dystrophy

  • Cerebromacular Degeneration

  • Ceroid-Lipofuscinosis

  • Ncl - [Neuronal Ceroid Lipofuscinosis]

  • Amaurotic Familial Idiocy

  • Amaurotic Idiocy

  • Amaurotic Idiot

  • Neuronal Lipofuscinosis

  • Pigmentary Retinal Lipoid Neuronal Heredodegeneration

Neuroblastoma
  • Nb

  • Neuroblastoma, Susceptibility To

  • Neuroblastomas

  • Central Neuroblastoma

Cerebral Amyloid Angiopathy, Itm2b-Related, 2
  • Dementia, Familial Danish

  • Fdd

  • Familial Danish Dementia

  • Heredopathia Ophthalmootoencephalica

  • Hooe

  • Cerebellar Ataxia, Cataract, Deafness, And Dementia Or Psychosis

  • Adan Amyloidosis

  • Itm2b-Related Cerebral Amyloid Angiopathy 2

  • Itm2b Amyloidosis

  • Familial Cerebral Amyloid Angiopathy

  • Itm2b-Related Amyloidosis

  • Itm2b-Related Cerebral Amyloid Angiopathy

  • Familial Dementia, Danish Type

  • Cerebral Amyloid Angiopathy, Itm2b-Related 2

  • CAA-ITM2B2

  • Cerebellar Ataxia Cataract Deafness And Dementia Or Psychosis

  • Dementia, Familial, Danish

Hereditary Ataxia
  • Sca

  • Spinocerebellar Ataxia

  • Ataxias Hereditary

  • Ataxias, Hereditary

Epilepsy
  • Epilepsy Syndrome

  • Epileptic Syndrome

  • Epilepsies

  • Symptomatic Epilepsies

  • Post Traumatic Epilepsy

  • Traumatic Epilepsy

  • Traumatic Epileptic

  • Epilepsy Due To Hippocampal Sclerosis

  • Epilepsy With Ammon'S Horn Sclerosis

  • Epilepsy Due To Cortical Dysplasia

  • Epilepsy Due To Neuronal Migration Disorders

Ischemia
  • Acute Coronary Syndrome

Hypertension, Essential
  • Essential Hypertension

  • Hypertension

  • High Blood Pressure

  • Hypertension, Essential, Susceptibility To

  • Hypertensive Disease

  • Primary Hypertension

  • EHT

  • Hypertension, Salt-Sensitive Essential, Susceptibility To

  • Hyperpiesia

  • Idiopathic Hypertension

  • Hypertensive Disorder

  • Hypertension, Essential, Susceptibility To, 3

  • Hypertension, Essential 3

  • Hypertension, Essential, Salt-Sensitive

  • Hypertension, Essential, Susceptibility To, 6

  • Hypertension, Essential 6

  • Hypertension, Salt-Sensitive Essential

  • Hypertension, Susceptibility To

  • Hypertension, Essential, Susceptibility To, 4

  • Hypertension, Essential 4

  • Hypertension, Essential, Susceptibility To, 2

  • Hypertension, Essential 2

  • Hypertension, Essential, Susceptibility To, 1

  • Hypertension, Essential 1

  • Hypertension, Essential, Susceptibility To, 5

  • Hypertension, Essential 5

  • Htn

  • Vascular Hypertensive Disorder

  • Systemic Primary Arterial Hypertension

  • Hbp - [High Blood Pressure]

  • Systemic Arterial Hypertensive Disorder

  • Elevated Blood Pressure

  • Arterial Hypertension Nos

  • Hypertension Nos

  • Benign Hypertension

  • Systemic Arterial Hypertension

  • Systemic Hypertension

  • Artery Htn

  • Benign Htn

  • Vascular Htn

  • Vascular Hypertension

  • Cholesterol Hypertension

  • Cholesterol Htn

  • Idiopathic Htn

  • Malignant Hypertension

  • Malignant Htn

  • Raised Blood Pressure

  • Cardiovascular Hypertension

  • Primary Htn - [Hypertension]

  • High Arterial Tension

  • High Blood Pressure Disorder

  • Ht - [Hypertension]

  • Htn - [Hypertension]

  • Hypertensive Vascular Disease

  • Hypertensive Vascular Degeneration

Bipolar Disorder
  • Bipolar Depression

  • Manic Disorder

  • Depression, Bipolar

  • Bipolar Disorder Manic Phase

  • Depressive-Manic Psych.

  • Manic Bipolar Affective Disorder

  • Manic Bipolar I Disorder

  • Manic Depression

  • Manic Depressive Disorder

  • Mixed Bipolar Disorder

  • Bipolar Affective Disorder

  • Bipolar Affective Psychosis

  • Bipolar Spectrum Disorder

  • Manic Depressive Illness

  • Depression Bipolar

  • Bipolar Disorder, Mixed

  • Major Affective Disorder

  • Major Affective Disorder 1

  • Major Affective Disorder 2

Congenital Nervous System Abnormality
  • Congenital Neurologic Anomaly

  • Congenital Nervous System Disorder

Central Nervous System Disease
  • CNS

  • Cns Diseases

  • Central Nervous System Diseases

  • Cns Disorder

Fatal Familial Insomnia
  • Insomnia, Fatal Familial

  • FFI

  • Familial Fatal Insomnia

  • Insomnia Familial Fatal

  • Insomnia Fatal Familial

  • Insomnia, Fatal, Familial

  • Ffi - [Fatal Familial Insomnia]

Binswanger'S Disease
  • Multi-Infarct Dementia

  • Dementia Multi-Infarct

  • Binswanger Disease

Eye Disease
  • Eye Diseases

  • Abnormality Of The Eye

  • Toxoplasma Oculopathy

Scrapie
Chromosomal Disease
  • Chromosomal Disorders

  • Congenital Chromosomal Disease

Niemann-Pick Disease, Type C1
  • Niemann-Pick Disease, Type C

  • NPC1

  • Niemann-Pick Disease, Type D

  • Niemann-Pick Disease Type C1

  • Niemann-Pick Disease With Cholesterol Esterification Block

  • Niemann-Pick Disease, Subacute Juvenile Form

  • Neurovisceral Storage Disease With Vertical Supranuclear Ophthalmoplegia

  • Npc

  • Niemann-Pick Disease, Chronic Neuronopathic Form

  • Niemann-Pick Disease Without Sphingomyelinase Deficiency

  • Niemann-Pick Disease Type C

  • Niemann-Pick Disease Type D

  • Niemann-Pick C1 Disease

  • Niemann-Pick Disease C1

  • Niemann-Pick Disease Chronic Neuronopathic Form

  • Niemann-Pick Disease Nova Scotian Type

  • Niemann-Pick Disease Subacute Juvenile Form

  • Niemann-Pick Disease Type Ii

  • Niemann-Picks Disease Type C

Pick Disease Of Brain
  • Pick Disease

  • Pick Disease Of The Brain

  • Lobar Atrophy Of Brain

  • Dementia With Lobar Atrophy And Neuronal Cytoplasmic Inclusions

  • Pick'S Disease

  • Behavioral Variant Of Frontotemporal Dementia

  • Dementia In Pick'S Disease

  • Lobar Atrophy Of The Brain

  • Bvftd

  • Bv-Ftd

  • PIDB

  • Picks Disease

Pervasive Developmental Disorder
  • Pervasive Development Disorder

  • Pervasive Developmental Disorders

  • Pervasive Child Development Disorders

  • Autistic Behavior

  • Autism Spectrum Disorders

Diabetic Encephalopathy
Toxic Encephalopathy
  • Neurotoxicity

  • Neurotoxicity Syndromes

  • Neurotoxicity Syndrome

  • Encephalopathy, Toxic

Mild Cognitive Impairment
C Syndrome
  • Opitz Trigonocephaly Syndrome

  • Trigonocephaly

  • Trigonocephaly Syndrome

  • Trigonocephaly C Syndrome

  • Opitz C Trigonocephaly

  • Opitz Trigonocephaly C Syndrome

  • Otcs

  • CSYN

Angioedema
  • Angioneurotic Oedema

  • Quincke'S Edema

  • Angioneurotic Edema

  • Giant Urticaria

Movement Disease
  • Movement Disorders

  • Movement Disorder

Postencephalitic Parkinson Disease
  • Postencephalitic Parkinsonism

  • Parkinson Disease, Postencephalitic

Attention Deficit-Hyperactivity Disorder
  • Attention Deficit Hyperactivity Disorder

  • ADHD

  • Attention Deficit Disorder

  • Attention Deficit-Hyperactivity Disorder, Susceptibility To

  • Attention Deficit Disorder With Hyperactivity

  • Hyperkinetic Disorder

  • Hyperactivity Of Childhood

  • Attention-Deficit/Hyperactivity Disorder

  • Add

  • Addh

  • Attention Deficit

  • Attention Deficit Disorder Of Childhood With Hyperactivity

  • Attention Deficit Disorder With Hyperactivity Syndrome

  • Hyperkinetic Syndrome

  • Attention-Deficit Hyperactivity Disorder

  • Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type

  • Disturbance Of Activity And Attention

  • Disorder Of Activity And Attention

  • Adhd - [Attention Deficit Hyperactivity Disorder]

  • Hyperkinetic Disorders

  • Disorder Of Activity And Attention With Hyperkinesia

  • Attention Deficit Syndrome With Hyperactivity

Arteriolosclerosis
Polycystic Lipomembranous Osteodysplasia With Sclerosing Leukoencephalopathy 1
  • Nasu-Hakola Disease

  • Polycystic Lipomembranous Osteodysplasia With Sclerosing Leukoencephalopathy

  • Plosl

  • Nhd

  • Presenile Dementia With Bone Cysts

  • Plo-Sl

  • PLOSL1

  • Dementia, Prefrontal, With Bone Cysts

  • Dementia, Progressive, With Lipomembranous Polycystic Osteodysplasia

  • Brain-Bone-Fat Disease

  • Progressive Dementia With Lipomembranous Polycystic Osteodysplasia

  • Brain-Bone-Fat Disease

Parkinson Disease, Late-Onset
  • Parkinson Disease

  • Parkinson'S Disease

  • PD

  • PARK

  • Parkinson Disease, Susceptibility To

  • Late Onset Parkinson'S Disease

  • Late Onset Parkinson Disease

  • Paralysis Agitans

  • Primary Parkinsonism

  • Idiopathic Parkinson Disease

  • Parkinson'S

  • Parkinson Disease, Late-Onset, Susceptibility To

  • Parkinson Disease, Age Of Onset, Modifier

  • Lewy Body Parkinson Disease

  • Idiopathic Parkinson'S Disease

  • Pd - [Parkinson Disease]

  • Parkinson Disease Nos

  • Parkinson, Nos

  • Primary Parkinson Disease

Fragile X Syndrome
  • FXS

  • Martin-Bell Syndrome

  • Fraxa Syndrome

  • Marker X Syndrome

  • X-Linked Mental Retardation And Macroorchidism

  • Fragile X Mental Retardation Syndrome

  • Fra Syndrome

  • Mental Retardation, X-Linked, Associated With Marxq28

  • Frax Syndrome

  • Symptomatic Form Of Fragile X Syndrome In Female Carriers

  • Fragile-X Syndrome

  • Fraxe Syndrome

Speech And Communication Disorders
  • Language Disorder

  • Communication Disorder

  • Language Disorders

  • Communication Disorders

  • Speech Language Disorder

  • Speech-Language Disorder

  • Communication Impairment

  • Speech And Language Disorder

Subjective Cognitive Decline
Cataract
  • Cataracts

  • Cat - [Cataract]

  • Cataract Form

  • Lens Opacity

  • Lens Opacities

Kuru
  • Kuru, Susceptibility To

  • Kuru Encephalopathy

  • Kuru Encephalitis

  • Kuru Disease

Actinobacillosis
Autosomal Dominant Cerebellar Ataxia
  • Spinocerebellar Ataxia

  • Adca

  • Pierre Marie Cerebellar Ataxia

  • Ataxia, Spinocerebellar

  • Sca

  • Autosomal Dominant Spinocerebellar Ataxia

  • Spinocerebellar Ataxias

Supranuclear Palsy, Progressive, 1
  • Progressive Supranuclear Palsy

  • Steele-Richardson-Olszewski Syndrome

  • Supranuclear Palsy, Progressive

  • Psp

  • Progressive Supranuclear Ophthalmoplegia

  • PSNP1

  • Familial Progressive Supranuclear Palsy

  • Richardson'S Syndrome

  • Psp Syndrome

  • Progressive Supranuclear Palsy 1

  • Supranuclear Palsy Progressive

  • Ophthalmoplegia, Supranuclear, Progressive

  • Steele-Richardson-Olszewksi Syndrome

Pineal Gland Astrocytoma
  • Pineal Astrocytic Tumor

Hemorrhage, Intracerebral
  • Intracerebral Hemorrhage

  • Hemorrhagic Stroke

  • ICH

  • Hemorrhage, Intracerebral, Susceptibility To

  • Stroke, Hemorrhagic

  • Stroke, Hemorrhagic, Susceptibility To

  • Brain Hemorrhage

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1
  • FTDALS1

  • Frontotemporal Dementia And/Or Motor Neuron Disease

  • Ftdmnd

  • Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia

  • Alsftd

  • Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis

  • Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-1

  • Frontotemporal Dementia With Motor Neuron Disease

  • Ftdals

  • Ftd-Als

  • Ftd-Mnd

  • Frontotemporal Dementia With Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis With Frontotemporal Dementia 1

  • Amyotrophic Lateral Sclerosis/Frontotemporal Dementia

  • Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia 1

  • Frontotemporal Lobar Degeneration

  • Grn-Related Frontotemporal Dementia

Choreatic Disease
  • Chorea

  • Hereditary Chorea

Down Syndrome
  • Trisomy 21

  • Complete Trisomy 21 Syndrome

  • Down'S Syndrome

  • Trisomy 21 Syndrome

  • Down'S Syndrome - Trisomy 21

  • Downs Syndrome

  • G Trisomy

  • 47,Xx,+21

  • 47,Xy,+21

  • Trisomy G

  • Down Syndrome, Susceptibility To

  • Chromosome 21 Trisomy

  • Trisomy 21 Nos

  • Abnormal Autosomes 21

Nervous System Disease
  • Abnormality Of The Nervous System

  • Nervous System Diseases

  • Nervous System Disorder

Disease Of Mental Health
  • Mental Health

  • Mental Disorders

Amnestic Disorder
  • Amnesia

  • Amnestic Syndrome

  • Korsakoff'S Psychosis Or Syndrome

  • Amnesic Syndrome

  • Amnestic Disorder In Conditions Classified Elsewhere

  • Korsakoff Psychosis Or Syndrome, Nonalcoholic

  • Nonalcoholic Organic Amnesic Syndrome

  • Organic Amnesic Syndrome

Cerebral Amyloid Angiopathy, App-Related
  • Hchwad

  • Amyloidosis, Cerebroarterial, App-Related

  • Amyloidosis, Hereditary, With Cerebral Hemorrhage, Dutch Variant

  • Cerebral Amyloid Angiopathy, App-Related, Dutch Variant

  • Cerebral Amyloid Angiopathy, App-Related, Iowa Variant

  • Cerebral Amyloid Angiopathy, App-Related, Italian Variant

  • Cerebral Amyloid Angiopathy, App-Related, Flemish Variant

  • Cerebral Amyloid Angiopathy, App-Related, Arctic Variant

  • Cerebral Amyloid Angiopathy, Dutch, Italian, Iowa, Flemish, Arctic Variants

  • App-Related Cerebral Amyloid Angiopathy

  • Abetaa21g Amyloidosis

  • Abeta Amyloidosis, Italian Type

  • Abeta Amyloidosis, Arctic Type

  • Abeta Amyloidosis, Iowa Type

  • Abeta Amyloidosis, Dutch Type

  • Hchwa-D

  • Abeta Amyloidosis, Flemish Type

  • Abetaa21g-Related Amyloidosis

  • Hchwa, Flemish Type

  • Hereditary Cerebral Hemorrhage With Amyloidosis, Flemish Type

  • Abetae22k Amyloidosis

  • Hchwa, Italian Type

  • Hereditary Cerebral Hemorrhage With Amyloidosis, Italian Type

  • Abetae22g Amyloidosis

  • Hchwa, Arctic Type

  • Hereditary Cerebral Hemorrhage With Amyloidosis, Arctic Type

  • Abetad23n Amyloidosis

  • Hchwa, Iowa Type

  • Hereditary Cerebral Hemorrhage With Amyloidosis, Iowa Type

  • Abetal34v Amyloidosis

  • Abeta Amyloidosis, Piedmont Type

  • Abetal34v-Related Amyloidosis

  • Hchwa, Piedmont Type

  • Hereditary Cerebral Hemorrhage With Amyloidosis, Piedmont Type

  • Abetae22q Amyloidosis

  • Hchwa, Dutch Type

  • Hereditary Cerebral Hemorrhage With Amyloidosis, Dutch Type

  • CAA-APP

  • Amyloidosis Cerebroarterial App-Related

  • Amyloidosis Hereditary With Cerebral Hemorrhage Dutch Variant

  • Cerebral Amyloid Angiopathy App-Related Arctic Variant

  • Cerebral Amyloid Angiopathy App-Related Dutch Variant

  • Cerebral Amyloid Angiopathy App-Related Flemish Variant

  • Cerebral Amyloid Angiopathy App-Related Iowa Variant

  • Cerebral Amyloid Angiopathy App-Related Italian Variant

  • Familial Occipital Calcifications With Hemorrhagic Strokes Leukoencephalopathy Arterial Dysplasia Dementia

  • Fochs-Ladd

  • Hereditary Cerebral Amyloid Angiopathy Dutch Type

  • Hereditary Cerebral Hemorrhage With Amyloidosis Dutch Type

  • Hereditary Cerebral Hemorrhage With Amyloidosis Italian Type

  • Cerebral Hemorrhage With Amyloidosis, Hereditary, Dutch Type

Amyotrophic Lateral Sclerosis 1
  • Amyotrophic Lateral Sclerosis

  • ALS

  • Lou Gehrig Disease

  • Amyotrophic Lateral Sclerosis Type 1

  • Charcot Disease

  • ALS1

  • Amyotrophic Lateral Sclerosis, Susceptibility To

  • Fals

  • Lou Gehrig'S Disease

  • Mnd

  • Motor Neuron Disease

  • Familial Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis 1, Familial

  • Amyotrophic Lateral Sclerosis 1, Autosomal Dominant

  • Motor Neuron Disease, Bulbar

  • Motor Neurone Disease

  • Amyotrophic Lateral Sclerosis With Dementia

  • Dementia With Amyotrophic Lateral Sclerosis

  • Motor Neuron Disease, Amyotrophic Lateral Sclerosis

  • Sclerosis, Lateral, Amyotrophic

  • Sclerosis, Lateral, Amyotrophic, Type 1

  • Amyotrophic Sclerosis

  • Als - [Amyotrophic Lateral Sclerosis]

  • Wasting Palsy

  • Amyotrophic Paralysis

  • Amyotrophy Lateral Sclerosis

  • Wasting Paralysis

  • Spinal Progressive Amyotrophy

  • Progressive Atrophic Paralysis

Amyloidosis, Hereditary, Transthyretin-Related
  • Transthyretin Amyloidosis

  • Familial Amyloid Polyneuropathy

  • Ttr Amyloid Neuropathy

  • Transthyretin Amyloid Neuropathy

  • Transthyretin Amyloid Polyneuropathy

  • Fap

  • Familial Transthyretin Amyloidosis

  • Amyloidosis Transthyretin Related

  • Type I Familial Amyloid Polyneuropathy

  • Familial Amyloid Polyneuropathy Type I

  • Attrv122i Amyloidosis

  • Hereditary Amyloidosis, Transthyretin-Related

  • Amyloid Polyneuropathy, Familial

  • Attr Amyloidosis

  • Attrm Amyloidosis

  • Corino De Andrade'S Disease

  • Paramyloidosis

  • Transthyretin-Related Hereditary Amyloidosis

  • Ttr Amyloidosis

  • Hereditary Attr Amyloidosis

  • Portuguese Polyneuritic Amyloidosis

  • Portuguese Type Familial Amyloid Neuropathy

  • Swiss Type Amyloid Polyneuropathy

  • Type Ii Familial Amyloid Polyneuropathy

  • Attrv30m Amyloidosis

  • Attrv30m-Related Amyloidosis

  • Familial Amyloid Polyneuropathy, Portuguese-Swedish-Japanese Type

  • Attr Cardiomyopathy

  • Attrv122i-Related Amyloidosis

  • Ttr-Related Amyloid Cardiomyopathy

  • Ttr-Related Cardiac Amyloidosis

  • Transthyretin Amyloid Cardiopathy

  • Transthyretin-Related Familial Amyloid Cardiomyopathy

  • Amyloidosis, Transthyretin-Related

  • AMYL-TTR

  • Amyloidosis I

  • Amyloidosis Ohio Type

  • Amyloidosis Type 7

  • Amyloidosis Vii

  • Amyloid Polyneuropathy

  • Attr

  • Familial Amyloid Polyneuropathy Type Ii

  • Hereditary Amyloidosis Transthyretin-Related

  • Leptomeningeal Amyloidosis

  • Meningocerebrovascular Amyloidosis

  • Oculoleptomeningeal Amyloidosis

  • Familial Amyloid Polyneuropathies

  • Amyloidosis, Leptomeningeal

  • Senile Cardiac Amyloidosis

  • Amyloid Neuropathies, Familial

  • Danish Type Familial Amyloid Cardiomyopathy

  • Familial Amyloid Neuropathy, Portuguese Type

  • Amyloid Polyneuropathy, Swiss Type

  • Hereditary Oculoleptomeningeal Amyloid Angiopathy

  • Amyloid Neuropathies

Niemann-Pick Disease
  • Sphingomyelin/Cholesterol Lipidosis

  • Niemann-Pick Diseases

  • Lipoid Histiocytosis

  • Sphingomyelin Lipidosis

  • Sphingomyelinase Deficiency Disease

  • Lipid Histiocytosis

  • Neuronal Cholesterol Lipidosis

  • Neuronal Lipidosis

  • Npd

  • Sphingomyelinase Deficiency

  • Niemann-Pick Disease, Type A

Peripheral Nervous System Neoplasm
  • Nerve Sheath Neoplasm

  • Peripheral Nervous System Neoplasms

  • Neoplasm Of Peripheral Nerve

  • Tumor Of Pns

  • Nerve Sheath Neoplasms

  • Nerve Sheath Tumors

Dementia
  • Dementias

  • Presenile Dementia

  • Alzheimer Type Dementia

  • Alzheimer Sclerosis

  • Alzheimer Disease Dementia

  • Alzheimer Dementia

  • Primary Degenerative Alzheimer Type Dementia

  • End Stage Alzheimer'S Dementia

  • Alzheimer'S Type Atypical Dementia

  • Alzheimer Type Presenile Dementia

  • Early Onset Alzheimer Dementia

  • Dementia In Alzheimer Disease Type 2

  • Dementia In Alzheimer Disease With Early Onset

  • Early Onset Alzheimer Type Dementia, Uncomplicated

  • Primary Degenerative Alzheimer Type Dementia, Early Onset

  • Primary Degenerative Alzheimer Type Dementia, Presenile Onset, Uncomplicated

  • Alzheimer Disease Dementia With Early Onset

  • Presenile Sclerosis

  • Presenile Brain Sclerosis

  • Presenile Alzheimer Brain Sclerosis

  • Late Onset Alzheimer Dementia

  • Dementia In Alzheimer Disease Type 1

  • Dementia In Alzheimer Disease With Late Onset

  • Primary Degenerative Alzheimer Type Dementia, Late Onset

  • Sdat - [Senile Dementia, Alzheimer Type]

  • Alzheimer Disease Dementia With Late Onset

  • Late Onset Alzheimer Brain Sclerosis

  • Senile Alzheimer Brain Disease

  • Senile Alzheimer Brain Sclerosis

  • Senile Primary Degenerative Alzheimer Type Dementia

  • Senile Dementia Of The Alzheimer Type

  • Arteriosclerotic Dementia

  • Strategic-Infarct Dementia

  • Post Stroke Dementia

  • Vascular Cognitive Impairment

  • Vascular Dementia

  • Dementia Of The Lewy Body Type

  • Dementia With Lewy Bodies

  • Sdlt - [Senile Dementia Of The Lewy Body Type]

  • Senile Dementia Of The Lewy Body Type

  • Alcohol-Related Dementia

  • Alcoholic Dementia Nos

  • Alcohol-Induced Dementia

  • Alcoholic Brain Syndrome

  • Chronic Alcoholic Brain Syndrome

  • Alcohol Dementia

  • Late Onset Alcoholic Psychosis

  • Residual And Late-Onset Alcohol-Induced Psychotic Disorder

  • Mental And Behavioural Disorders Due To Use Of Sedatives Or Hypnotics, Residual And Late-Onset Psychotic Disorder

  • Late-Onset Psychoactive Substance-Induced Psychotic Disorder

  • Inhalant Dementia

  • Volatile Solvents Dementia

  • Dementia In Paralysis Agitans

  • Pdd - [Parkinson Disease Dementia]

  • Dementia Syndrome Of Parkinson Disease

  • Dementia In Parkinson Disease

  • Parkinson Related Dementia

  • Dementia In Huntington Chorea

  • Hiv - [Human Immunodeficiency Virus] Dementia

  • Hiv- [Human Immunodeficiency Virus] Associated Cognitive Motor Complex

  • Hiv- [Human Immunodeficiency Virus] Associated Dementia Complex

  • Aids - [Acquired Immunodeficiency Syndrome] Dementia Complex

  • Aids Related Dementia

  • Dementia Due To Niacin Deficiency

Residual Stage Of Open Angle Glaucoma
  • Open-Angle Glaucoma Residual Stage

Alzheimer Disease, Familial, 1
  • Alzheimer Disease

  • Alzheimer'S Disease

  • Presenile And Senile Dementia

  • AD1

  • Alzheimer Disease, Susceptibility To

  • Alzheimer Disease, Late-Onset, Susceptibility To

  • Alzheimer Disease 1, Familial

  • AD

  • Familial Alzheimer Disease

  • Alzheimer Disease, Late-Onset

  • Alzheimers Dementia

  • Alzheimer Dementia

  • Alzheimer Sclerosis

  • Alzheimer Syndrome

  • Alzheimer-Type Dementia

  • Dat

  • Primary Senile Degenerative Dementia

  • Sdat

  • Alzheimer Disease 1

  • Autosomal Dominant Alzheimer Disease

  • Early-Onset Alzheimer Disease With Cerebral Amyloid Angiopathy

  • Late Onset Alzheimer Disease

  • Alzheimers Disease

  • Alzheimer Disease, Early-Onset, With Cerebral Amyloid Angiopathy

  • Late-Onset Alzheimers Disease

  • Alzheimer'S Disease Pathway Kegg

  • Dementia Due To Alzheimer'S Disease

  • Alzheimer Disease Type 1

  • Alzheimers

Anxiety
  • Anxiety Disorder

  • Anxiety Disorders

  • Anxiety State

  • Anxieties

  • Anxiety Neurosis

Spinocerebellar Ataxia 1
  • Spinocerebellar Ataxia Type 1

  • SCA1

  • Olivopontocerebellar Atrophy I

  • Opca1

  • Opca4

  • Menzel Type Opca

  • Schut-Haymaker Type Opca

  • Spinocerebellar Atrophy I

  • Opca I

  • Olivopontocerebellar Atrophy Iv

  • Opca Iv

  • Cerebelloparenchymal Disorder I

  • Cpd1

  • Olivopontocerebellar Atrophy 1

  • Cerebelloparenchymal Disorder 1

  • Olivopontocerebellar Atrophy 4

  • Spinocerebellar Atrophy 1

  • Type 1 Spinocerebellar Ataxia

  • Spinocerebellar Ataxia-1

  • Ataxia, Spinocerebellar, Type 1

Aceruloplasminemia
  • Cerebellar Ataxia

  • Hypoceruloplasminemia

  • Hemosiderosis, Systemic, Due To Aceruloplasminemia

  • Familial Apoceruloplasmin Deficiency

  • Hereditary Ceruloplasmin Deficiency

  • Deficiency Of Ferroxidase

  • Hypoceruloplasminemia, Hereditary

  • Ceruloplasmin Deficiency

  • Systemic Hemosiderosis Due To Aceruloplasminemia

  • ACERULOP

Cerebrovascular Disease
  • Cerebrovascular Accident

  • Cerebrovascular Disorder

  • Cerebrovascular Disorders

  • Cva

  • Stroke

Hereditary Cerebral Amyloid Angiopathy
  • Cerebral Amyloid Angiopathy, Hereditary

  • Autosomal Dominant Cerebrovascular Amyloidosis

  • Caa, Familial

  • Cerebral Amyloid Angiopathy, Familial

  • Cerebral Amyloid Angiopathy, Genetic

  • Hchwa-D

  • Hchwa-I

  • Hereditary Cerebral Hemorrhage With Amyloidosis-Dutch Type

  • Hereditary Cerebral Hemorrhage With Amyloidosis-Icelandic Type

  • Familial Cerebral Amyloid Angiopathy

Aphasia
Type 2 Diabetes Mellitus
  • Insulin Resistance

  • NIDDM

  • Diabetes Mellitus, Non-Insulin-Dependent

  • Type 2 Diabetes

  • T2D

  • Noninsulin-Dependent Diabetes Mellitus

  • Diabetes Mellitus, Type Ii

  • Maturity-Onset Diabetes

  • Insulin Resistance, Severe, Digenic

  • Diabetes Mellitus, Type 2

  • Diabetes Mellitus, Noninsulin-Dependent

  • Diabetes Mellitus, Noninsulin-Dependent, Association With

  • Diabetes Mellitus, Noninsulin-Dependent, Late Onset

  • Hypertension, Insulin Resistance-Related, Susceptibility To

  • Insulin Resistance, Susceptibility To

  • Non-Insulin-Dependent Diabetes Mellitus

  • Type Ii Diabetes Mellitus

  • Adult-Onset Diabetes Mellitus

  • Maturity-Onset Diabetes Mellitus

  • Diabetes Mellitus Type 2

  • Type Ii Diabetes

  • Type 2 Diabetes Mellitus, Susceptibility To

  • Diabetes, Type 2

  • Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To

  • Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To

  • Diabetes Mellitus, Type 2, Susceptibility To

  • Diabetes Mellitus, Noninsulin-Dependent, 2

  • Diabetes Mellitus, Type Ii, Susceptibility To

  • Hypertension, Insulin Resistance-Related

  • Adult-Onset Diabetes

  • Aodm

  • Diabetes Mellitus, Adult-Onset

  • Diabetes Mellitus Type Ii

  • Diabetes Mellitus Type 2, Susceptibility To

  • Diabetes, Type Ii, Susceptibility To

  • Diabetes Type 2

  • Diabetes Mellitus

  • Adult Onset Diabetes

  • Maturity Onset Diabetes

  • Nonketotic Diabetes

  • Non-Insulin Dependent Diabetes Mellitus

  • T2dm - [Type 2 Diabetes Mellitus]

  • Niddm - [Non Insulin Dependent Diabetes Mellitus]

  • Dm2

  • Dm Type Ii

  • Diabetic Type 2

  • Insulin Requiring Type 2 Diabetes

  • Noninsulin Dependent Diabetes

  • Non-Insulin-Dependent Diabetes Mellitus Without Complications

  • Diabetes Due To Insulin Secretory Defect

  • Diabetes Mellitus Due To Insulin Secretory Defect

  • Non-Insulin-Dependent Diabetes Of The Young

  • Senile Diabetes

  • Nonketotic Hyperglycaemia

  • Stable Diabetes

Autonomic Nervous System Neoplasm
  • Tumor Of Autonomic Nervous System

Vascular Dementia
  • Dementia, Vascular

  • Multi Infarct Dementia

  • Multifocal Dementia

  • Dementia Vascular

  • Vascular Dementia, Susceptibility To

  • Dementia, Multi-Infarct

  • Multi-Infarct Dementia

Visual Agnosia
  • Primary Visual Agnosia

Peripheral Nervous System Disease
  • Peripheral Neuropathy

  • Peripheral Nerve Disease

  • Peripheral Nerve Disorders

  • Neuropathy, Peripheral

  • Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation

Parkinsonism
  • Parkinsonism-Plus

  • Idiopathic Parkinsonism

  • Primary Parkinsonism

  • Paralysis Agitans Syndrome

  • Parkinsonian Syndrome

  • Trembling Paralysis

  • Paralysis Agitans

  • Shaking Palsy

  • Shaking Paralysis

Psychotic Disorder
  • Psychotic Disorders

  • Mental Or Behavioural Disorder

  • Psychotic

  • Mental Disorders

Creutzfeldt-Jakob Disease
  • Variant Creutzfeldt-Jakob Disease

  • CJD

  • Bovine Spongiform Encephalopathy

  • Vcjd

  • Inherited Creutzfeldt-Jakob Disease

  • Creutzfeldt-Jakob Disease, Familial

  • Creutzfeldt Jakob Disease

  • Creutzfeldt-Jacob Disease

  • Creutzfeldt Jacob Disease

  • Sporadic Creutzfeldt-Jakob Disease

  • Encephalopathy, Bovine Spongiform

  • Creutzfeldt-Jakob Disease, Variant, Resistance To

  • Creutzfeldt-Jakob Disease, Variant

  • Creutzfeldt Jacob Syndrome

  • Jakob-Creutzfeldt Disease

  • Subacute Spongiform Encephalopathy

  • Transmissible Virus Dementia

  • New Variant Of Cjd

  • Nv-Cjd

  • Variant Cjd

  • Variant Creutzfeldt-Jacob Disease

  • Sporadic Cjd

  • Inherited Cjd

  • Acquired Creutzfeldt-Jakob Disease

  • Variant Mcj

  • Encephalopathy Bovine Spongiform

  • Familial Creutzfeldt-Jakob Disease

  • Creutzfeldt-Jakob Syndrome

  • New Variant Creutzfeldt-Jakob Disease

  • Creutzfeldt-Jakob Disease, Sporadic

  • Acquired Cjd

  • Scjd - [Sporadic Creutzfeldt-Jakob Disease]

  • Idiopathic Creutzfeldt-Jakob Disease

  • Creutzfeld-Jakob Disease Nos

  • Vcjd - [Variant Creutzfeldt-Jakob Disease]

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Bos taurus APP VGNC VGNC:26038
Mus musculus APP MGD MGI:88059
Felis catus APP VGNC VGNC:67880
Rattus norvegicus APP RGD RGD:2139
Macaca mulatta APP VGNC VGNC:80791
Canis familiaris APP VGNC VGNC:38010
Others APP NCBI