SOD1 - superoxide dismutase 1 Gene

Also Known as ALS; SOD; ALS1; IPOA; STAHP; hSod1; HEL-S-44; homodimer

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 6647

About SOD1

Cytogenetic location: 21q22.11 Genomic coordinates (GRCh38): 21:31,659,693-31,668,931 (from NCBI)

This gene has 4 transcripts (splice variants), 229 orthologues, 2 paralogues and is associated with 3 phenotypes. Ubiquitous expression in liver (RPKM 426.2), kidney (RPKM 226.6) and 23 other tissues.

Summary

The protein encoded by this gene binds copper and zinc ions and is one of two isozymes responsible for destroying free superoxide radicals in the body. The encoded isozyme is a soluble cytoplasmic protein, acting as a homodimer to convert naturally-occuring but harmful superoxide radicals to molecular oxygen and hydrogen peroxide. The Other isozyme is a mitochondrial protein. In addition, this protein contains an antimicrobial peptide that displays Antibacterial, Antifungal, and anti-MRSA activity against E. coli, E. faecalis, S. aureus, S. aureus MRSA LPV+, S. agalactiae, and yeast C. krusei. Mutations in this gene have been implicated as causes of familial amyotrophic lateral sclerosis. Rare transcript variants have been reported for this gene. [provided by RefSeq, Jul 2020]

SOD1 Products (1)

mRNA Protein Name
NM_000454.5 NP_000445.1 superoxide dismutase [Cu-Zn]

Gene Ontology

  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence References Source
enables copper ion binding IDA
IDA: Inferred from direct assay
17008312 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
17592131 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
12968035 GOA
enables protein homodimerization activity IPI
IPI: Inferred from physical interaction
24567322 GOA
enables protein phosphatase 2B binding IDA
IDA: Inferred from direct assay
17324120 GOA
enables protein-folding chaperone binding IPI
IPI: Inferred from physical interaction
9726962 GOA
enables small GTPase binding IDA
IDA: Inferred from direct assay
18219391 GOA
enables superoxide dismutase activity IDA
IDA: Inferred from direct assay
12551919 GOA
enables zinc ion binding IDA
IDA: Inferred from direct assay
17381088 GOA
Biological Process GO Annotation Evidence References Source
involved in heart contraction IDA
IDA: Inferred from direct assay
9539776 GOA
involved in hydrogen peroxide biosynthetic process IDA
IDA: Inferred from direct assay
15544046 GOA
involved in positive regulation of cytokine production IDA
IDA: Inferred from direct assay
15544046 GOA
involved in positive regulation of oxidative stress-induced intrinsic apoptotic signaling pathway IMP
IMP: Inferred from mutant phenotype
12551919 GOA
involved in positive regulation of superoxide anion generation IDA
IDA: Inferred from direct assay
18219391 GOA
involved in reactive oxygen species metabolic process IDA
IDA: Inferred from direct assay
24140062 GOA
involved in regulation of GTPase activity IDA
IDA: Inferred from direct assay
18219391 GOA
involved in regulation of mitochondrial membrane potential IMP
IMP: Inferred from mutant phenotype
16790527 GOA
involved in removal of superoxide radicals IDA
IDA: Inferred from direct assay
16254550 GOA
involved in response to superoxide IDA
IDA: Inferred from direct assay
16790527 GOA
involved in superoxide metabolic process IDA
IDA: Inferred from direct assay
12551919 GOA
Cellular Component GO Annotation Evidence References Source
located in cytoplasm IDA
IDA: Inferred from direct assay
1332049 GOA
located in cytoplasmic vesicle IDA
IDA: Inferred from direct assay
17077646 GOA
located in cytosol IDA
IDA: Inferred from direct assay
16790527 GOA
located in dendrite cytoplasm IDA
IDA: Inferred from direct assay
17324120 GOA
located in extracellular space IDA
IDA: Inferred from direct assay
9453566 GOA
located in mitochondrion IDA
IDA: Inferred from direct assay
16790527 GOA
located in neuronal cell body IDA
IDA: Inferred from direct assay
17324120 GOA
located in nucleus IDA
IDA: Inferred from direct assay
1332049 GOA
located in peroxisome IDA
IDA: Inferred from direct assay
1332049 GOA
colocalizes with plasma membrane IDA
IDA: Inferred from direct assay
17077646 GOA
part of protein-containing complex IDA
IDA: Inferred from direct assay
17324120 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

SOD1 Protein Structure

Sod_Cu

Sod_Cu: Copper/zinc superoxide dismutase (SODC) (5 - 150)

  • 0
  • 100
  • 154 a.a.
Protein Preferred Names Protein Names

superoxide dismutase [Cu-Zn]

  • Cu/Zn superoxide dismutase

SOD1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
SOD1 P00441 SGSM1 Homo sapiens Q2NKQ1-4
Y2H Array
32814053
Intra
SOD1 P00441 SGSM1 Homo sapiens Q2NKQ1-4
Y2H Pooling
32814053
Intra
SOD1 P00441 SGSM1 Homo sapiens Q2NKQ1-4
Validated Y2H
32814053
Intra
SOD1 P00441 ARL16 Homo sapiens Q0P5N6
Y2H Pooling
32814053
Intra
SOD1 P00441 ARL16 Homo sapiens Q0P5N6
Validated Y2H
32814053
Intra
SOD1 P00441 ARL16 Homo sapiens Q0P5N6
Y2H Array
32814053
Intra
SOD1 P00441 PBX4 Homo sapiens Q9BYU1
Y2H Pooling
32814053
Intra
SOD1 P00441 PBX4 Homo sapiens Q9BYU1
Validated Y2H
32814053
Intra
SOD1 P00441 PBX4 Homo sapiens Q9BYU1
Y2H Array
32814053
Intra
SOD1 P00441 TMX1 Homo sapiens Q9H3N1
Validated Y2H
32814053
Intra
SOD1 P00441 TMX1 Homo sapiens Q9H3N1
Y2H Pooling
32814053
Intra
SOD1 P00441 TMX1 Homo sapiens Q9H3N1
Y2H Array
32814053
Intra
SOD1 P00441 OTUB1 Homo sapiens Q96FW1
Y2H Array
32814053
Intra
SOD1 P00441 OTUB1 Homo sapiens Q96FW1
Validated Y2H
32814053
Intra
SOD1 P00441 OTUB1 Homo sapiens Q96FW1
Y2H Pooling
32814053
Intra
SOD1 P00441 C6orf141 Homo sapiens Q5SZD1
Y2H Pooling
32814053
Intra
SOD1 P00441 C6orf141 Homo sapiens Q5SZD1
Validated Y2H
32814053
Intra
SOD1 P00441 C6orf141 Homo sapiens Q5SZD1
Y2H Array
32814053
Intra
SOD1 P00441 KLHL36 Homo sapiens Q8N4N3-2
Y2H Pooling
32814053
Intra
SOD1 P00441 KLHL36 Homo sapiens Q8N4N3-2
Validated Y2H
32814053
Intra
SOD1 P00441 KLHL36 Homo sapiens Q8N4N3-2
Y2H Array
32814053
Intra
SOD1 P00441 TPM2 Homo sapiens P07951-2
Validated Y2H
32814053
Intra
SOD1 P00441 TPM2 Homo sapiens P07951-2
Y2H Array
32814053
Intra
SOD1 P00441 TPM2 Homo sapiens P07951-2
Y2H Pooling
32814053
Intra
SOD1 P00441 LDHAL6B Homo sapiens Q9BYZ2
Validated Y2H
32814053
Intra
SOD1 P00441 LDHAL6B Homo sapiens Q9BYZ2
Y2H Array
32814053
Intra
SOD1 P00441 LDHAL6B Homo sapiens Q9BYZ2
Y2H Pooling
32814053
Intra
SOD1 P00441 SP6 Homo sapiens Q3SY56
Validated Y2H
32814053
Intra
SOD1 P00441 SP6 Homo sapiens Q3SY56
Y2H Array
32814053
Intra
SOD1 P00441 SP6 Homo sapiens Q3SY56
Y2H Pooling
32814053
Intra
SOD1 P00441 AP2B1 Homo sapiens P63010-2
Y2H Array
32814053
Intra
SOD1 P00441 AP2B1 Homo sapiens P63010-2
Y2H Pooling
32814053
Intra
SOD1 P00441 AP2B1 Homo sapiens P63010-2
Validated Y2H
32814053
Intra
SOD1 P00441 CCS Homo sapiens O14618
Anti Tag CoIP
33961781
Intra
SOD1 P00441 CCS Homo sapiens O14618
TAP
24981860
Intra
SOD1 P00441 CCS Homo sapiens O14618
Anti Tag CoIP
28514442
Intra
SOD1 P00441 DAB2 Homo sapiens P98082
Validated Y2H
32814053
Intra
SOD1 P00441 DAB2 Homo sapiens P98082
Y2H Array
32814053
Intra
SOD1 P00441 DAB2 Homo sapiens P98082
Y2H Pooling
32814053
Intra
SOD1 P00441 PPP3CA Homo sapiens Q08209-2
Validated Y2H
32814053
Intra
SOD1 P00441 PPP3CA Homo sapiens Q08209-2
Y2H Array
32814053
Intra
SOD1 P00441 PPP3CA Homo sapiens Q08209-2
Y2H Pooling
32814053
Intra
SOD1 P00441 L3MBTL3 Homo sapiens Q96JM7-2
Y2H Array
32814053
Intra
SOD1 P00441 L3MBTL3 Homo sapiens Q96JM7-2
Validated Y2H
32814053
Intra
SOD1 P00441 L3MBTL3 Homo sapiens Q96JM7-2
Y2H Pooling
32814053
Intra
SOD1 P00441 ZSCAN1 Homo sapiens Q8NBB4-2
Y2H Array
32814053
Intra
SOD1 P00441 ZSCAN1 Homo sapiens Q8NBB4-2
Validated Y2H
32814053
Intra
SOD1 P00441 ZSCAN1 Homo sapiens Q8NBB4-2
Y2H Pooling
32814053
Intra
SOD1 P00441 IFI35 Homo sapiens P80217-2
Y2H Array
32814053
Intra
SOD1 P00441 IFI35 Homo sapiens P80217-2
Y2H Pooling
32814053
Intra
SOD1 P00441 IFI35 Homo sapiens P80217-2
Validated Y2H
32814053
Intra
SOD1 P00441 RNF19A Homo sapiens Q9NV58
Y2H Pooling
32814053
Intra
SOD1 P00441 RNF19A Homo sapiens Q9NV58
Validated Y2H
32814053
Intra
SOD1 P00441 RNF19A Homo sapiens Q9NV58
Y2H Array
32814053
Intra
SOD1 P00441 ZXDC Homo sapiens Q2QGD7
Validated Y2H
32814053
Intra
SOD1 P00441 ZXDC Homo sapiens Q2QGD7
Y2H Array
32814053
Intra
SOD1 P00441 ZXDC Homo sapiens Q2QGD7
Y2H Pooling
32814053
Intra
SOD1 P00441 FGA Homo sapiens Q8WW76
Validated Y2H
32814053
Intra
SOD1 P00441 FGA Homo sapiens Q8WW76
Y2H Pooling
32814053
Intra
SOD1 P00441 FGA Homo sapiens Q8WW76
Y2H Array
32814053
Intra
SOD1 P00441 PSMC4 Homo sapiens P43686-2
Validated Y2H
32814053
Intra
SOD1 P00441 PSMC4 Homo sapiens P43686-2
Y2H Array
32814053
Intra
SOD1 P00441 PSMC4 Homo sapiens P43686-2
Y2H Pooling
32814053
Intra
SOD1 P00441 RNF111 Homo sapiens Q6ZNA4-2
Validated Y2H
32814053
Intra
SOD1 P00441 RNF111 Homo sapiens Q6ZNA4-2
Y2H Array
32814053
Intra
SOD1 P00441 RNF111 Homo sapiens Q6ZNA4-2
Y2H Pooling
32814053
Intra
SOD1 P00441 SYMPK Homo sapiens Q92797-2
Validated Y2H
32814053
Intra
SOD1 P00441 SYMPK Homo sapiens Q92797-2
Y2H Array
32814053
Intra
SOD1 P00441 SYMPK Homo sapiens Q92797-2
Y2H Pooling
32814053
Intra
SOD1 P00441 IQSEC1 Homo sapiens Q6DN90-2
Y2H Pooling
32814053
Intra
SOD1 P00441 IQSEC1 Homo sapiens Q6DN90-2
Validated Y2H
32814053
Intra
SOD1 P00441 IQSEC1 Homo sapiens Q6DN90-2
Y2H Array
32814053
Intra
SOD1 P00441 LNX2 Homo sapiens Q8N448
Y2H Array
32814053
Intra
SOD1 P00441 LNX2 Homo sapiens Q8N448
Y2H Pooling
32814053
Intra
SOD1 P00441 LNX2 Homo sapiens Q8N448
Validated Y2H
32814053
Intra
SOD1 P00441 TNFAIP1 Homo sapiens Q13829
Y2H Array
32814053
Intra
SOD1 P00441 TNFAIP1 Homo sapiens Q13829
Validated Y2H
32814053
Intra
SOD1 P00441 TNFAIP1 Homo sapiens Q13829
Y2H Pooling
32814053
Intra
SOD1 P00441 MPND Homo sapiens Q8N594
Validated Y2H
32814053
Intra
SOD1 P00441 MPND Homo sapiens Q8N594
Y2H Array
32814053
Intra
SOD1 P00441 MPND Homo sapiens Q8N594
Y2H Pooling
32814053
Intra
SOD1 P00441 ANXA8 Homo sapiens P13928
Y2H Pooling
32814053
Intra
SOD1 P00441 ANXA8 Homo sapiens P13928
Validated Y2H
32814053
Intra
SOD1 P00441 ANXA8 Homo sapiens P13928
Y2H Array
32814053
Intra
SOD1 P00441 RNF112 Homo sapiens Q9ULX5
Y2H Pooling
32814053
Intra
SOD1 P00441 RNF112 Homo sapiens Q9ULX5
Validated Y2H
32814053
Intra
SOD1 P00441 RNF112 Homo sapiens Q9ULX5
Y2H Array
32814053
Intra
SOD1 P00441 OTUD7B Homo sapiens Q6GQQ9-2
Y2H Pooling
32814053
Intra
SOD1 P00441 OTUD7B Homo sapiens Q6GQQ9-2
Validated Y2H
32814053
Intra
SOD1 P00441 OTUD7B Homo sapiens Q6GQQ9-2
Y2H Array
32814053
Intra
SOD1 P00441 TERF2 Homo sapiens Q15554-4
Validated Y2H
32814053
Intra
SOD1 P00441 TERF2 Homo sapiens Q15554-4
Y2H Array
32814053
Intra
SOD1 P00441 TERF2 Homo sapiens Q15554-4
Y2H Pooling
32814053
Intra
SOD1 P00441 HNRNPLL Homo sapiens Q8WVV9-3
Y2H Pooling
32814053
Intra
SOD1 P00441 HNRNPLL Homo sapiens Q8WVV9-3
Validated Y2H
32814053
Intra
SOD1 P00441 HNRNPLL Homo sapiens Q8WVV9-3
Y2H Array
32814053
Intra
SOD1 P00441 CAMKK1 Homo sapiens Q8N5S9-2
Validated Y2H
32814053
Intra
SOD1 P00441 CAMKK1 Homo sapiens Q8N5S9-2
Y2H Array
32814053
Intra
SOD1 P00441 CAMKK1 Homo sapiens Q8N5S9-2
Y2H Pooling
32814053
Intra
SOD1 P00441 KBTBD4 Homo sapiens Q9NVX7-2
Y2H Array
32814053
Intra
SOD1 P00441 KBTBD4 Homo sapiens Q9NVX7-2
Validated Y2H
32814053
Intra
SOD1 P00441 KBTBD4 Homo sapiens Q9NVX7-2
Y2H Pooling
32814053
Intra
SOD1 P00441 ZMAT2 Homo sapiens Q96NC0
Validated Y2H
32814053
Intra
SOD1 P00441 ZMAT2 Homo sapiens Q96NC0
Y2H Array
32814053
Intra
SOD1 P00441 ZMAT2 Homo sapiens Q96NC0
Y2H Pooling
32814053
Intra
SOD1 P00441 SF3B3 Homo sapiens Q15393
Validated Y2H
32814053
Intra
SOD1 P00441 SF3B3 Homo sapiens Q15393
Y2H Array
32814053
Intra
SOD1 P00441 SF3B3 Homo sapiens Q15393
Y2H Pooling
32814053
Intra
SOD1 P00441 GPSM3 Homo sapiens Q9Y4H4
Y2H Array
32814053
Intra
SOD1 P00441 GPSM3 Homo sapiens Q9Y4H4
Validated Y2H
32814053
Intra
SOD1 P00441 GPSM3 Homo sapiens Q9Y4H4
Y2H Pooling
32814053
Intra
SOD1 P00441 TUBB Homo sapiens P07437
Y2H Array
32814053
Intra
SOD1 P00441 TUBB Homo sapiens P07437
Y2H Pooling
32814053
Intra
SOD1 P00441 TUBB Homo sapiens P07437
Validated Y2H
32814053
Intra
SOD1 P00441 GAPDH Homo sapiens P04406
Anti Bait CoIP
29128334
Intra
SOD1 P00441 RPSA Homo sapiens P08865
Validated Y2H
32814053
Intra
SOD1 P00441 RPSA Homo sapiens P08865
Y2H Pooling
32814053
Intra
SOD1 P00441 RPSA Homo sapiens P08865
Y2H Array
32814053
Intra
SOD1 P00441 KARS1 Homo sapiens Q15046
Validated Y2H
32814053
Intra
SOD1 P00441 KARS1 Homo sapiens Q15046
Y2H Array
32814053
Intra
SOD1 P00441 KARS1 Homo sapiens Q15046
Y2H Pooling
32814053
Intra
SOD1 P00441 GNB2 Homo sapiens P62879
Y2H Pooling
32814053
Intra
SOD1 P00441 GNB2 Homo sapiens P62879
Validated Y2H
32814053
Intra
SOD1 P00441 GNB2 Homo sapiens P62879
Y2H Array
32814053
Intra
SOD1 P00441 PSMC1 Homo sapiens P62191
Validated Y2H
32814053
Intra
SOD1 P00441 PSMC1 Homo sapiens P62191
Y2H Array
32814053
Intra
SOD1 P00441 PSMC1 Homo sapiens P62191
Crosslink
29128334
Intra
SOD1 P00441 PSMC1 Homo sapiens P62191
Y2H Pooling
32814053
Intra
SOD1 P00441 SKIC8 Homo sapiens Q9GZS3
Y2H Array
32814053
Intra
SOD1 P00441 SKIC8 Homo sapiens Q9GZS3
Y2H Pooling
32814053
Intra
SOD1 P00441 SKIC8 Homo sapiens Q9GZS3
Validated Y2H
32814053
Intra
SOD1 P00441 EEF1D Homo sapiens P29692
Crosslink
29128334
Intra
SOD1 P00441 PSMC3 Homo sapiens P17980
Y2H Array
32814053
Intra
SOD1 P00441 PSMC3 Homo sapiens P17980
Y2H Pooling
32814053
Intra
SOD1 P00441 PSMC3 Homo sapiens P17980
Validated Y2H
32814053
Intra
SOD1 P00441 RPP25 Homo sapiens Q9BUL9
Y2H Array
32814053
Intra
SOD1 P00441 RPP25 Homo sapiens Q9BUL9
Validated Y2H
32814053
Intra
SOD1 P00441 RPP25 Homo sapiens Q9BUL9
Y2H Pooling
32814053
Intra
SOD1 P00441 PSMB8 Homo sapiens P28062-2
Y2H Pooling
32814053
Intra
SOD1 P00441 PSMB8 Homo sapiens P28062-2
Validated Y2H
32814053
Intra
SOD1 P00441 PSMB8 Homo sapiens P28062-2
Y2H Array
32814053
Intra
SOD1 P00441 HOXC4 Homo sapiens P09017
Validated Y2H
32814053
Intra
SOD1 P00441 HOXC4 Homo sapiens P09017
Y2H Array
32814053
Intra
SOD1 P00441 HOXC4 Homo sapiens P09017
Y2H Pooling
32814053
Intra
SOD1 P00441 UBB Homo sapiens P0CG47
Validated Y2H
32814053
Intra
SOD1 P00441 UBB Homo sapiens P0CG47
Y2H Array
32814053
Intra
SOD1 P00441 UBB Homo sapiens P0CG47
Y2H Pooling
32814053
Intra
SOD1 P00441 MGARP Homo sapiens Q8TDB4
Validated Y2H
32814053
Intra
SOD1 P00441 MGARP Homo sapiens Q8TDB4
Y2H Array
32814053
Intra
SOD1 P00441 MGARP Homo sapiens Q8TDB4
Y2H Pooling
32814053
Intra
SOD1 P00441 BAK1 Homo sapiens Q16611
Validated Y2H
32814053
Intra
SOD1 P00441 BAK1 Homo sapiens Q16611
Y2H Pooling
32814053
Intra
SOD1 P00441 BAK1 Homo sapiens Q16611
Y2H Array
32814053
Intra
SOD1 P00441 RBBP4 Homo sapiens Q09028
Validated Y2H
32814053
Intra
SOD1 P00441 RBBP4 Homo sapiens Q09028
Y2H Pooling
32814053
Intra
SOD1 P00441 RBBP4 Homo sapiens Q09028
Y2H Array
32814053
Intra
SOD1 P00441 C9 Homo sapiens P02748
Validated Y2H
32814053
Intra
SOD1 P00441 C9 Homo sapiens P02748
Y2H Array
32814053
Intra
SOD1 P00441 C9 Homo sapiens P02748
Y2H Pooling
32814053
Intra
SOD1 P00441 SPATA22 Homo sapiens Q8NHS9
Y2H Pooling
32814053
Intra
SOD1 P00441 SPATA22 Homo sapiens Q8NHS9
Validated Y2H
32814053
Intra
SOD1 P00441 SPATA22 Homo sapiens Q8NHS9
Y2H Array
32814053
Intra
SOD1 P00441 PDZK1IP1 Homo sapiens Q13113
Y2H Pooling
32814053
Intra
SOD1 P00441 PDZK1IP1 Homo sapiens Q13113
Validated Y2H
32814053
Intra
SOD1 P00441 PDZK1IP1 Homo sapiens Q13113
Y2H Array
32814053
Intra
SOD1 P00441 PRDX5 Homo sapiens P30044
Anti Bait CoIP
29128334
Intra
SOD1 P00441 PRDX5 Homo sapiens P30044
Crosslink
29128334
Intra
SOD1 P00441 PRDX5 Homo sapiens P30044
Anti Tag CoIP
29128334
Intra
SOD1 P00441 CBLB Homo sapiens Q13191
Validated Y2H
32814053
Intra
SOD1 P00441 CBLB Homo sapiens Q13191
Y2H Pooling
32814053
Intra
SOD1 P00441 CBLB Homo sapiens Q13191
Y2H Array
32814053
Intra
SOD1 P00441 STAC3 Homo sapiens Q96MF2
Validated Y2H
32814053
Intra
SOD1 P00441 STAC3 Homo sapiens Q96MF2
Y2H Pooling
32814053
Intra
SOD1 P00441 STAC3 Homo sapiens Q96MF2
Y2H Array
32814053
Intra
SOD1 P00441 CRYBA2 Homo sapiens P53672
Validated Y2H
32814053
Intra
SOD1 P00441 CRYBA2 Homo sapiens P53672
Y2H Array
32814053
Intra
SOD1 P00441 CRYBA2 Homo sapiens P53672
Y2H Pooling
32814053
Intra
SOD1 P00441 RYBP Homo sapiens Q8N488
Y2H Array
32814053
Intra
SOD1 P00441 RYBP Homo sapiens Q8N488
Y2H Pooling
32814053
Intra
SOD1 P00441 RYBP Homo sapiens Q8N488
Validated Y2H
32814053
Intra
SOD1 P00441 TBL1XR1 Homo sapiens Q9BZK7
Validated Y2H
32814053
Intra
SOD1 P00441 TBL1XR1 Homo sapiens Q9BZK7
Y2H Array
32814053
Intra
SOD1 P00441 TBL1XR1 Homo sapiens Q9BZK7
Y2H Pooling
32814053
Cross
SOD1 P00441 Hspa5 Mus musculus P20029
Anti Bait CoIP
16595634
Cross
SOD1 P00441 Hspa5 Mus musculus P20029
Anti Tag CoIP
19171884
Cross
SOD1 P00441 Hspa5 Mus musculus P20029
Pull Down
16595634
Intra
SOD1 P00441 BCL2 Homo sapiens P10415
Validated Y2H
32814053
Intra
SOD1 P00441 BCL2 Homo sapiens P10415
Y2H Pooling
32814053
Intra
SOD1 P00441 BCL2 Homo sapiens P10415
Y2H Array
32814053
Intra
SOD1 P00441 SEM1 Homo sapiens P60896
Validated Y2H
32814053
Intra
SOD1 P00441 SEM1 Homo sapiens P60896
Y2H Pooling
32814053
Intra
SOD1 P00441 SEM1 Homo sapiens P60896
Y2H Array
32814053
Intra
SOD1 P00441 DYNC2LI1 Homo sapiens Q8TCX1
Pull Down
21252941
Intra
SOD1 P00441 CSNK1D Homo sapiens P48730-2
Y2H Array
32814053
Intra
SOD1 P00441 CSNK1D Homo sapiens P48730-2
Y2H Pooling
32814053
Intra
SOD1 P00441 CSNK1D Homo sapiens P48730-2
Validated Y2H
32814053
Intra
SOD1 P00441 ENKUR Homo sapiens Q8TC29
Validated Y2H
32814053
Intra
SOD1 P00441 ENKUR Homo sapiens Q8TC29
Y2H Array
32814053
Intra
SOD1 P00441 ENKUR Homo sapiens Q8TC29
Y2H Pooling
32814053
Intra
SOD1 P00441 FGA Homo sapiens P02671-2
Y2H Array
32814053
Intra
SOD1 P00441 FGA Homo sapiens P02671-2
Y2H Pooling
32814053
Intra
SOD1 P00441 FGA Homo sapiens P02671-2
Validated Y2H
32814053
Intra
SOD1 P00441 SNCA Homo sapiens P37840
SLC
26643113
Intra
SOD1 P00441 SNCA Homo sapiens P37840
Crosslink
26643113
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
NMR
19369197
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
Solution Sedimentation
21257910
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
Comigration in SDS
19022905
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
GMS
19022905
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
Aggregation
31999698
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
Light Scattering
17592131
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
Filter Trap
31999698
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
TEM
19022905
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
DLS
21257910
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
SLCA
17592131
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
X-Ray Diffraction
19369197
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
Biophysical
23831581
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
Solution Sedimentation
23831581
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
Fluorescence Spectr
19022905
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
GMS
19171884
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
GMS
17592131
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
SLC
26643113
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
SLCA
19022905
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
TEM
23831581
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
NMR
19828437
Intra
SOD1 P00441 SOD1 Homo sapiens P00441
Fluorescence Spectr
17592131
Cross
SOD1 P00441 Chgb Mus musculus P16014
Anti Tag CoIP
16369483
Cross
SOD1 P00441 Chgb Mus musculus P16014
Anti Bait CoIP
16369483
Cross
SOD1 P00441 Chgb Mus musculus P16014
Y2H
16369483
Cross
SOD1 P00441 Chga Mus musculus P26339
Anti Tag CoIP
16369483
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant SOD1 Proteins

Cat. No. Product Name Accession Purity
HY-P71048 SOD1 Protein, Human (His) P00441 (M1-Q154) ≥ 95%, as determined by reducing SDS-PAGE.

SOD1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P81228 SOD-1 Antibody (YA3541) WB, IHC-P, ICC/IF, FC Human, Mouse, Rat
HY-P83888 SOD-1 Antibody (YA3585) WB, ICC/IF, FC, ELISA Human, Mouse
HY-P83888A SOD-1 Antibody (YA3585)(PBS only) WB, ICC/IF, FC, ELISA Human, Mouse
HY-P85373 SOD-1 Antibody (YA5065) WB; IHC-P; IHC-F; ICC/IF; IF-Tissue; FC Human, Rat, Mouse
HY-P86424 SOD-1 Antibody (YA6116) WB, IHC-P, ICC/IF, IP, ELISA Human, Mouse, Rat

Related Diseases

Diseases Alias
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
Spastic Tetraplegia And Axial Hypotonia, Progressive

  • STAHP

  • Sod1 Deficiency, Autosomal Recessive
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
Lateral Sclerosis

  • Primary Lateral Sclerosis

  • Adult-Onset Primary Lateral Sclerosis

  • Adult-Onset Pls

  • Motor Neuron Disease

  • Pls

  • Pls - [Primary Lateral Sclerosis]

  • Lateral Spinal Sclerosis

  • Lateral Complete Paralysis

  • Lateral Incomplete Paralysis

  • Lateral Paralysis
Eales Disease

  • Idiopathic Obliterative Vasculopathy

  • Idiopathic Recurrent Vitreal Hemorrhage

  • Idiopathic Retinal Perivasculitis

  • Idiopathic Retinal Vasculitis
Senile Cataract
Mild Pre-Eclampsia

  • Mild Toxemia
Pneumoconiosis

  • Pneumoconioses

  • Silicosis Nos

  • Complicated Silicosis

  • Fibrosis Of Lung With Silicosis

  • Nodular Silicosis

  • Pneumoconiosis Due To Silica

  • Silicotic Fibrosis Of Lung

  • Simple Silicosis

  • Silicatosis

  • Silicotic Lung Fibrosis

  • Pneumoconiosis Due To Talc

  • Pulmonary Talcosis

  • Talc Lung Disease

  • Talc Pneumoconiosis

  • Talc Workers' Pneumoconiosis

  • Talcosis

  • Fibrosis Of Lung Due To Talc

  • Asbestos Pneumoconiosis

  • Amianthosis

  • Asbestosis

  • Lung Fibrosis With Asbestosis

  • Pulmonary Asbestosis
Bronchopulmonary Dysplasia

  • Bpd
Acne

  • Acne Vulgaris

  • Acne Varioliformis

  • Frontalis Acne
Postcholecystectomy Syndrome

  • Post Cholecystectomy Syndrome
Spinal And Bulbar Muscular Atrophy, X-Linked 1

  • Kennedy Disease

  • Sbma

  • Spinal And Bulbar Muscular Atrophy

  • Kennedy'S Disease

  • X-Linked Spinal And Bulbar Muscular Atrophy

  • SMAX1

  • Kd

  • Kennedy Spinal And Bulbar Muscular Atrophy

  • Spinobulbar Muscular Atrophy

  • Bulbospinal Muscular Atrophy, X-Linked

  • Bulbospinal Neuronopathy, X-Linked Recessive

  • Xbsn

  • Spinal And Bulbar Muscular Atrophy Of Kennedy

  • Bulbospinal Muscular Atrophy

  • X-Linked Bulbospinal Amyotrophy

  • Bulbo-Spinal Atrophy, X-Linked

  • Spinal Bulbar Muscular Atrophy

  • X-Linked Bulbo-Spinal Atrophy

  • X-Linked Spinal Bulbar Muscular Atrophy

  • X-Linked Bsma

  • X-Linked Bulbospinal Muscular Atrophy

  • Spinal And Bulbar Muscular Atrophy X-Linked 1

  • Bulbospinal Muscular Atrophy X-Linked

  • Bulbospinal Neuronopathy X-Linked Recessive

  • Kennedy Disease)

  • Kennedy Syndrome

  • Atrophy, Muscular, Spinal And Bulbar, Kennedy Type

  • Atrophy, Muscular, Spinobulbar

  • Bulbospinal Neuronopathy
Wilson Disease

  • Hepatolenticular Degeneration

  • WD

  • Wilson'S Disease

  • WND

  • Westphal-Strumpell Syndrome

  • Copper Storage Disease

  • Cerebral Pseudosclerosis

  • Westphal Pseudosclerosis

  • Hepatolenticular Degeneration Syndrome

  • Copper Retention

  • Hepatocerebral Degeneration

  • Kinnier-Wilson Disease

  • Neurohepatic Degeneration

  • Progressive Hepatolenticular Degeneration

  • Lenticular Degenerative Disease

  • Wilson'S Syndrome

  • Lenticular Syndrome
Ischemia

  • Acute Coronary Syndrome
Tonsillitis

  • Chronic Tonsillitis

  • Throat Infection - Tonsillitis
Brain Edema

  • Cerebral Edema

  • Intracranial Swelling

  • Wet Brain
Myocardial Stunning
Amyotrophic Lateral Sclerosis 19

  • Amyotrophic Lateral Sclerosis Type 19

  • ALS19

  • Sclerosis, Lateral, Amyotrophic, Type 19
Septooptic Dysplasia

  • Septo-Optic Dysplasia

  • De Morsier Syndrome

  • Growth Hormone Deficiency With Pituitary Anomalies

  • SOD

  • Pituitary Hormone Deficiency, Combined, 5

  • Septo-Optic Dysplasia Spectrum

  • Septo-Optic Dysplasia With Growth Hormone Deficiency

  • Pituitary Hormone Deficiency, Combined 5

  • Hypopituitarism And Septooptic 'Dysplasia'

  • GHDPA

  • CPHD5

  • Dysplasia, Septo-Optic

  • Kallmann Syndrome
Spinal Cord Neuroblastoma

  • Neuroblastoma Of The Spinal Cord
Spinal Cord Primitive Neuroectodermal Neoplasm

  • Spinal Cord Pnet

  • Spinal Cord Primitive Neuroectodermal Tumor
Friedreich Ataxia

  • Friedreich Ataxia 1

  • FRDA

  • Friedreich Ataxia With Retained Reflexes

  • Frda1

  • Fa

  • Friedreich'S Ataxia

  • Hereditary Spinal Ataxia

  • Fa1

  • Friedreich'S Tabes

  • Hereditary Spinal Sclerosis

  • Spinocerebellar Ataxia, Friedreich

  • Friedreich Spinocerebellar Ataxia

  • Friedrich'S Ataxia
Methemoglobinemia
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
Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia

  • Amyotrophic Lateral Sclerosis Type 10

  • ALS10

  • Amyotrophic Lateral Sclerosis 10, With Or Without Ftd

  • Frontotemporal Lobar Degeneration, Tardbp-Related

  • Amyotrophic Lateral Sclerosis 10

  • Amyotrophic Lateral Sclerosis 10, With Or Without Frontotemporal Dementia

  • Tardbp-Related Frontotemporal Lobar Degeneration With Tdp43 Inclusions

  • Amyotrophic Lateral Sclerosis 10 With Or Without Frontotemporal Dementia And With Tdp43 Inclusions

  • Sclerosis, Lateral, Amyotrophic, Type Type 10
Spinocerebellar Ataxia 2

  • Spinocerebellar Ataxia Type 2

  • SCA2

  • Amyotrophic Lateral Sclerosis 13

  • Spinocerebellar Degeneration With Slow Eye Movements

  • SDSEM

  • Spinocerebellar Atrophy Ii

  • Olivopontocerebellar Atrophy Ii

  • Opca2

  • Cerebellar Degeneration With Slow Eye Movements

  • Wadia-Swami Syndrome

  • Amyotrophic Lateral Sclerosis Type 13

  • ALS13

  • Olivopontocerebellar Atrophy Holguin Type

  • Spinocerebellar Ataxia Cuban Type

  • Olivopontocerebellar Atrophy, Holguin Type

  • Spinocerebellar Ataxia, Cuban Type

  • Amyotrophic Lateral Sclerosis, Susceptibility To, 13

  • Olivopontocerebellar Atrophy 2

  • Sca 2

  • Spinocerebellar Ataxia With Slow Eye Movements

  • Spinocerebellar Atrophy 2

  • Wadia Swami Syndrome

  • Opca Ii

  • Spinocerebellar Ataxia-2

  • Ataxia, Spinocerebellar, Type 2
Hyperekplexia

  • Hereditary Hyperekplexia

  • Kok Disease

  • Congenital Stiff Man Syndrome

  • Familial Startle Disease

  • Sthe

  • Stiff-Baby Syndrome

  • Hereditary Hyperexplexia

  • Startle Disease

  • Exaggerated Startle Reaction

  • Hyperexplexia Hereditary

  • Startle Disease, Familial

  • Startle Reaction, Exaggerated

  • Stiff-Man Syndrome, Congenital

  • Stiff-Person Syndrome, Congenital

  • Congenital Stiff-Man Syndrome

  • Congenital Stiff-Person Syndrome

  • Familial Hyperekplexia

  • Startle Syndrome

  • Stiff Baby Syndrome

  • Hyperekplexia, Hereditary

  • Stiff-Person Syndrome
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
Amyotrophic Lateral Sclerosis Type 6

  • Amyotrophic Lateral Sclerosis 6, Autosomal Recessive

  • Als6

  • Amyotrophic Lateral Sclerosis 6, With Or Without Frontotemporal Dementia

  • Autosomal Recessive Amyotrophic Lateral Sclerosis 6

  • Sclerosis, Lateral, Amyotrophic, Type Type 6

  • Amyotrophic Lateral Sclerosis 6
Amyotrophic Lateral Sclerosis 4, Juvenile

  • Amyotrophic Lateral Sclerosis Type 4

  • ALS4

  • Amyotrophic Lateral Sclerosis 4

  • Dhmn With Upper Motor Neuron Signs

  • Distal Hereditary Motor Neuropathy With Upper Motor Neuron Signs

  • Neuronopathy, Distal Hereditary Motor, With Pyramidal Features

  • Als 4

  • Distal Hereditary Motor Neuropathy With Pyramidal Features

  • Amyotrophic Lateral Sclerosis Juvenile 4

  • Neuronopathy Distal Hereditary Motor With Pyramidal Features

  • Sclerosis, Lateral, Amyotrophic, Type Type 4
Uremia

  • Uremia Of Renal Origin
Hyperhomocysteinemia
Retinal Vasculitis
Amyotrophic Lateral Sclerosis 2, Juvenile

  • ALS2

  • Als, Juvenile

  • Alsj

  • Amyotrophic Lateral Sclerosis Type 2

  • Amyotrophic Lateral Sclerosis 2

  • Amyotrophic Lateral Sclerosis Type 2, Juvenile

  • Amyotrophic Lateral Sclerosis Juvenile

  • Amyotrophic Lateral Sclerosis Juvenile 2

  • Sclerosis, Lateral, Amyotrophic, Type Type 2
Hyperglycemia
Amyotrophic Lateral Sclerosis 20

  • Amyotrophic Lateral Sclerosis Type 20

  • ALS20

  • Sclerosis, Lateral, Amyotrophic, Type 20
Vascular Disease

  • Vascular Diseases

  • Aneurysm

  • Spinal Cord Ischemia

  • Vascular Anomaly

  • Spinal Cord Vascular Diseases

  • Vascular Tissue Disease
Charcot-Marie-Tooth Disease, Axonal, Type 2e

  • Charcot-Marie-Tooth Disease Type 2

  • CMT2E

  • CMT2S

  • CMT2Y

  • Charcot-Marie-Tooth Disease Type 2e

  • Charcot-Marie-Tooth Disease Type 2y

  • Charcot-Marie-Tooth Disease Axonal Type 2s

  • Charcot-Marie-Tooth Disease, Axonal, Type 2s

  • Charcot-Marie-Tooth Disease, Type 2e

  • Hereditary Motor And Sensory Neuropathy Type 2

  • Charcot-Marie-Tooth Neuropathy, Type 2s

  • Charcot-Marie-Tooth Disease, Axonal, Autosomal Recessive, Type 2s

  • Charcot-Marie-Tooth Disease, Axonal, Type 2y

  • Charcot-Marie-Tooth Disease, Axonal, Autosomal Dominant, Type 2y

  • Charcot-Marie-Tooth Neuropathy, Type 2y

  • Charcot-Marie-Tooth Disease, Type 2y

  • Autosomal Dominant Charcot-Marie-Tooth Disease Type 2e

  • Charcot-Marie-Tooth Neuropathy Type 2e

  • Autosomal Dominant Charcot-Marie-Tooth Disease Type 2 Due To Vcp Mutation

  • Cmt2 Due To Vcp Mutation

  • Charcot-Marie-Tooth Disease Type 2s

  • Autosomal Dominant Charcot-Marie-Tooth Disease Type 2

  • Autosomal Dominant Axonal Charcot-Marie-Tooth Disease

  • Cmt2

  • Charcot-Marie-Tooth Neuropathy, Type 2e

  • Hereditary Motor And Sensory Neuropathy Guadalajara Neuronal Type

  • Hereditary Motor And Sensory Neuropathy Okinawa Type

  • Autosomal Dominant Axonal Charcot-Marie-Tooth Type 2y

  • Charcot-Marie-Tooth Neuropathy Type 2y

  • Autosomal Recessive Axonal Charcot-Marie-Tooth Type 2s

  • Charcot-Marie-Tooth Neuropathy Type 2s

  • Charcot-Marie-Tooth Type 2

  • Autosomal Dominant Charcot-Marie-Tooth Disease Type 2y

  • Charcot-Marie-Tooth Disease 2e

  • Charcot-Marie-Tooth Disease Axonal Type 2e

  • Charcot-Marie-Tooth Disease Neuronal Type 2e

  • Charcot-Marie-Tooth Disease 2s

  • Charcot-Marie-Tooth Neuropathy Axonal Type 2s

  • Charcot-Marie-Tooth Disease 2y

  • Charcot-Marie-Tooth Disease, Type 2

  • Hereditary Motor And Sensory-Neuropathy Type Ii
Progressive Muscular Atrophy

  • Progressive Spinal Muscular Atrophy

  • Pure Progressive Muscular Atrophy

  • Pma

  • Hereditary Spinal Muscle Atrophy

  • Pma - [Progressive Muscular Atrophy]

  • Progressive Muscle Atrophy

  • Progressive Spinal Muscle Atrophy

  • Duchenne-Aran Atrophy

  • Duchenne-Aran Muscle Atrophy

  • Hereditary Sma - [Spinal Muscle Atrophy]
Amyotrophic Lateral Sclerosis 8

  • Amyotrophic Lateral Sclerosis Type 8

  • ALS8

  • Sclerosis, Lateral, Amyotrophic, Type Type 8
Progressive Bulbar Palsy

  • Bulbar Palsy, Progressive

  • Progressive Bulbar Atrophy

  • Bulbar Palsy

  • Pbp - [Progressive Bulbar Palsy]

  • Progressive Bulbar Paralysis

  • Bulbar Paralysis

  • Chronic Bulbar Palsy

  • Chronic Bulbar Paralysis

  • Supranuclear Bulbar Paralysis
Pancreatitis

  • Mumps Pancreatitis
Menkes Disease

  • Copper Transport Disease

  • Menkes Syndrome

  • MNK

  • Kinky Hair Disease

  • Steely Hair Disease

  • Menkes Kinky-Hair Syndrome

  • Mk

  • Steely Hair Syndrome

  • Menkea Syndrome

  • Md

  • Menkes Kinky Hair Syndrome

  • Hypocupremia, Congenital

  • Kinky Hair Syndrome

  • X-Linked Copper Deficiency

  • Menkes Kinky Hair Disease
Keratoconus

  • Kc

  • Conical Cornea

  • Noninflammatory Corneal Thining

  • Bulging Cornea

  • Cornea Conical

  • Acquired Conus Of Cornea
Varicocele

  • Scrotal Varices

  • Varicoceles

  • Varicocele Of Scrotum

  • Scrotal Varicocele
Erysipelas
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 4

  • FTDALS4

  • Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-4

  • Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis, Type 4
Pre-Eclampsia

  • Preeclampsia

  • Gestational Hypertension

  • Hypertension Induced By Pregnancy

  • Pre-Eclamptic Toxaemia

  • Pregnancy Associated Hypertension

  • Proteinuric Hypertension Of Pregnancy

  • Hypertension, Pregnancy-Induced, Susceptibility To

  • Preeclampsia/Eclampsia

  • Pregnancy Toxemia

  • Toxaemia Of Pregnancy

  • Gestational Proteinuric Hypertension

  • Pregnancy-Induced Hypertension

  • Toxemia Of Pregnancy

  • Preeclampsia, Susceptibility To

  • Transient Hypertension Of Pregnancy

  • Gestational [Pregnancy-Induced] Hypertension Without Significant Proteinuria

  • Gestational Hypertension Nos

  • Mild Proteinuric Hypertension Of Pregnancy

  • Pih - [Pregnancy-Induced Hypertension]

  • Pregnancy-Induced Hypertension Nos

  • Gestational [Pregnancy-Induced] Hypertension With Significant Proteinuria

  • Pe - [Pre-Eclampsia]

  • Pre-Eclampsia Nos

  • Pre-Eclamptic Nos

  • Pregnancy Pre-Eclampsia

  • Puerperal Pre-Eclampsia

  • Pre-Eclampsia Toxaemia

  • Toxaemia In Pregnancy

  • Pet - [Pre-Eclamptic Toxaemia]

  • Maternal Toxaemia
Porphyria, Acute Intermittent

  • Acute Intermittent Porphyria

  • Porphobilinogen Deaminase Deficiency

  • Pbgd Deficiency

  • AIP

  • Porphyria, Swedish Type

  • Uroporphyrinogen Synthase Deficiency

  • Ups Deficiency

  • Porphyria, Acute Intermittent, Nonerythroid Variant

  • Hydroxymethylbilane Synthase Deficiency

  • Aip - Acute Intermittent Porphyria

  • Porphyria Intermittent Acute

  • Pyrroloporphyria

  • Hmbs Deficiency

  • Porphyria Acute Intermittent
Acute Pancreatitis

  • Pancreatitis

  • Pancreatitis, Acute Necrotizing

  • Pancreatitis Nos

  • Acute Pancreas Inflammation
Lung Disease

  • Lung Diseases

  • Disorder Of Lung

  • Abnormality Of The Lung
Exfoliation Syndrome

  • Pseudoexfoliation Glaucoma

  • Pseudoexfoliation Syndrome

  • Exfoliation Syndrome, Susceptibility To

  • XFS

  • Exfoliation Glaucoma

  • Xfg

  • Pseudoexfoliation Of The Lens

  • Pexg

  • Pexs

  • Exfoliative Syndrome

  • Glaucoma Capsulare

  • Pex

  • Pseudo-Exfoliation Syndrome
Atrophic Gastritis

  • Gastritis, Atrophic

  • Gastric Atrophy

  • Gastritis Atrophic
Amyotrophic Lateral Sclerosis 11

  • Amyotrophic Lateral Sclerosis Type 11

  • ALS11

  • Sclerosis, Lateral, Amyotrophic, Type Type 11
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
Locked-In Syndrome

  • Locked In Syndrome

  • Cerebromedullospinal Disconnection

  • Locked-In State

  • Quadriplegia
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
Bacterial Meningitis

  • Meningitis, Bacterial

  • Meningitis Bacterial

  • Bm - [Bacterial Meningitis]

  • Leptomeningitis Bacterial

  • Pachymeningitis Bacterial

  • Arachnoiditis Bacterial
Amyotrophic Lateral Sclerosis 18

  • Amyotrophic Lateral Sclerosis Type 18

  • ALS18

  • Sclerosis, Lateral, Amyotrophic, Type 18
Male Infertility

  • Infertility, Male

  • Infertility Male

  • Male Sterility

  • Absolute Infertility
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]
Amyotrophic Lateral Sclerosis 16, Juvenile

  • Amyotrophic Lateral Sclerosis Type 16

  • ALS16

  • Amyotrophic Lateral Sclerosis 16

  • Sclerosis, Lateral, Amyotrophic, Type 16, Juvenile
Amyotrophic Lateral Sclerosis Type 12

  • Amyotrophic Lateral Sclerosis 12

  • Als12

  • Sclerosis, Lateral, Amyotrophic, Type Type 12
Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1

  • Guam Disease

  • Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex Of Guam

  • Als-Pdc

  • Lytico-Bodig Disease

  • Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Complex

  • Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex 1, Susceptibility To

  • Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex, Susceptibility To

  • Amyotrophic Lateral Sclerosis-Parkinsonism/Dementia Complex

  • Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Of Guam Syndrome

  • Parkinsonism-Dementia-Als Complex

  • Pdals

  • Amyotrophic Lateral Sclerosis, Parkinsonism/Dementia Complex Of Guam

  • Parkinson-Dementia Complex Of Guam

  • G-Pdc

  • Guam Parkinsonism-Dementia Complex

  • ALS-PDC1

  • Als/Pdc Of Guam

  • Amyotrophic Lateral Sclerosis

  • Sclerosis, Lateral, Amyotrophic/Parkinsonism/Dementia Complex 1

  • Amyotrophic Lateral Sclerosis, Guam Form

  • Parkinsonian Disorders
Maple Syrup Urine Disease

  • MSUD

  • Bckd Deficiency

  • Branched-Chain Ketoaciduria

  • Branched-Chain Alpha-Keto Acid Dehydrogenase Deficiency

  • Keto Acid Decarboxylase Deficiency

  • Maple Syrup Urine Disease, Type Ii

  • Branched Chain Ketoaciduria

  • Classic Maple Syrup Urine Disease

  • Intermittent Maple Syrup Urine Disease

  • Maple Syrup Urine Disease, Type Ia

  • Ketoacidaemia

  • Bckdh Deficiency

  • Branched-Chain 2-Ketoacid Dehydrogenase Deficiency

  • Thiamine-Responsive Maple Syrup Urine Disease

  • Intermediate Maple Syrup Urine Disease

  • Maple Syrup Urine Disease Type 1a

  • Maple Syrup Urine Disease Type 1b

  • Maple Syrup Urine Disease Type 2

  • Maple Syrup Urine Disease, Type Ib

  • Dihydrolipoamide Dehydrogenase Deficiency

  • Branched-Chain Ketoacid Dehydrogenase Deficiency

  • Maple Syrup Disease

  • Ketoacidemia

  • Classic Bckd Deficiency

  • Classic Msud

  • Classic Branched-Chain Alpha-Ketoacid Dehydrogenase Deficiency

  • Classic Branched-Chain Ketoaciduria

  • Thiamine-Responsive Bckd Deficiency

  • Thiamine-Responsive Msud

  • Thiamine-Responsive Branched-Chain Alpha-Ketoacid Dehydrogenase Deficiency

  • Intermittent Bckd Deficiency

  • Intermittent Msud

  • Intermittent Branched-Chain Alpha-Ketoacid Dehydrogenase Deficiency

  • Maple Syrup Urine Disease 1a

  • MSUD1A

  • Maple Syrup Urine Disease Type Ia

  • Msud Type Ia

  • Maple Syrup Urine Disease 1b

  • MSUD1B

  • Maple Syrup Urine Disease Type Ib

  • Msud Type Ib

  • Maple Syrup Urine Disease 2

  • MSUD2

  • Maple Syrup Urine Disease Type Ii

  • Msud Type Ii

  • Nadh Cytochrome B5 Reductase Deficiency

  • Lactic Acidosis, Congenital Infantile, Due To Lad Deficiency

  • Ketonemia

  • Maple Syrup Urine Disease, Type 1b

  • Ketoacid Decarboxylase Deficiency

  • Oxoacid Decarboxylase Deficiency

  • Branched Chain Ketoacid Dehydrogenase Deficiency

  • Msud - [Maple-Syrup-Urine Disease]

  • Ketoaminoacidaemia

  • Bckd - [Branched-Chain Alpha-Ketoacid Dehydrogenase Deficiency]

  • Maple-Syrup-Urine Disorder

  • Maple-Syrup-Urine Syndrome
Tetanus

  • Lockjaw

  • Clostridial Tetanus

  • Infection Due To Clostridium Tetani

  • Lock-Jaw
Cataract

  • Cataracts

  • Cat - [Cataract]

  • Cataract Form

  • Lens Opacity

  • Lens Opacities
Diabetes Mellitus

  • Diabetes
Spinal Muscular Atrophy

  • Sma

  • 5q Sma

  • Proximal Sma

  • Sma-Associated Sma

  • Spinal Amyotrophies

  • Spinal Amyotrophy

  • Spinal Muscle Degeneration

  • Spinal Muscle Wasting

  • Muscular Atrophy Spinal

  • Atrophy, Muscular, Spinal

  • Hereditary Motor Neuronopathy

  • Progressive Muscular Atrophy

  • Sma - [Spinal Muscular Atrophy]
Chronic Granulomatous Disease

  • Cgd

  • Granulomatous Disease, Chronic

  • Autosomal Recessive Chronic Granulomatous Disease

  • X-Linked Chronic Granulomatous Disease

  • Bridges-Good Syndrome

  • Congenital Dysphagocytosis

  • Quie Syndrome

  • Chronic Septic Granulomatosis

  • Chronic Granulomatous Disorder

  • Granulomatous Disease Chronic

  • Granulomatous Disease, Chronic, X-Linked
Type 2 Diabetes Mellitus

  • Insulin Resistance

  • NIDDM

  • Type 2 Diabetes

  • Diabetes Mellitus, Non-Insulin-Dependent

  • 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
Peyronie Disease
Amyotrophic Lateral Sclerosis Type 15

  • Amyotrophic Lateral Sclerosis 15, With Or Without Frontotemporal Dementia

  • Als15

  • Amyotrophic Lateral Sclerosis 15
Amyotrophic Lateral Sclerosis 21

  • Amyotrophic Lateral Sclerosis Type 21

  • ALS21

  • Multisystem Proteinopathy 5

  • Msp5

  • Distal Myopathy With Vocal Cord Weakness

  • Vcpdm

  • Myopathy, Distal, 2, Formerly

  • Mpd2, Formerly

  • Vocal Cord And Pharyngeal Dysfunction With Distal Myopathy, Formerly

  • Vcpdm, Formerly

  • Vocal Cord And Pharyngeal Distal Myopathy

  • Matr3-Related Distal Myopathy

  • Distal Myopathy 2

  • Mpd2

  • Vocal Cord And Pharyngeal Dysfunction With Distal Myopathy

  • Sclerosis, Lateral, Amyotrophic, Type 21

  • Myopathy, Distal 2
Hypotonia
Constipation
Postpoliomyelitis Syndrome

  • Postpolio Syndrome

  • Post-Polio Syndrome

  • Post Polio Syndrome

  • Polio Late Effects

  • Post-Polio Muscular Atrophy

  • Post-Polio Sequelae

  • Post-Poliomyelitic Syndrome

  • Postpolio Sequelae

  • Postpoliomyelitic Syndrome

  • Postpoliomyelitis Sequelae
Viral Hepatitis

  • Animal Viral Hepatitis

  • Hepatitis, Viral, Animal

  • Human Viral Hepatitis

  • Viral Hepatitis With Hepatic Coma
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
Platelet Aggregation, Spontaneous
Pseudobulbar Palsy

  • Pseudobulbar Paralysis
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
Beta-Thalassemia

  • Beta Thalassemia

  • Cooley'S Anemia

  • Mediterranean Anemia

  • Beta Thalassemia Intermedia

  • Erythroblastic Anemia

  • Thalassemia, Hispanic Gamma-Delta-Beta

  • Thalassemia Major

  • Thalassemia Minor

  • Beta-Plus-Thalassemia

  • Thalassemia, Beta

  • Beta Thalassemia Major

  • Beta Thalassemia Minor

  • Thalassemias, Beta-

  • Microcytemia, Beta Type

  • Thalassemia, Beta Type

  • B-THAL

  • Mediterranean Anaemia

  • Beta Thalassaemia Syndrome

  • Mediterranean Disease

  • Beta Thalassaemia Disease
Amyotrophic Lateral Sclerosis Type 14

  • Als14

  • Amyotrophic Lateral Sclerosis 14

  • Amyotrophic Lateral Sclerosis, With Or Without Frontotemporal Dementia

  • Amyotrophic Lateral Sclerosis 14 With Or Without Frontotemporal Dementia
Glycogen Storage Disease

  • Glycogenosis

  • Glycogenoses

  • Gsd

  • Storage Disease, Glycogen

  • Gsd - [Glycogen Storage Disease]

  • Glycogen Thesaurismosis

  • Diffuse Glycogenosis

  • Generalised Glycogen Storage Disease

  • Generalised Glycogenosis

  • Generalised Glycogen Storage Disease Of Infants

  • Glycogen Synthase Deficiency
Shigellosis

  • Dysentery, Bacillary

  • Bacillary Dysentery

  • Shigella Boydii Infectious Disease

  • Shigella Flexneri Infectious Disease

  • Shigella Gastroenteritis

  • Shigella Sonnei Infectious Disease

  • Shigella Infections
Fatal Familial Insomnia

  • Insomnia, Fatal Familial

  • FFI

  • Familial Fatal Insomnia

  • Insomnia Familial Fatal

  • Insomnia Fatal Familial

  • Insomnia, Fatal, Familial

  • Ffi - [Fatal Familial Insomnia]
Toxic Encephalopathy

  • Neurotoxicity

  • Neurotoxicity Syndromes

  • Neurotoxicity Syndrome

  • Encephalopathy, Toxic
Chromosomal Duplication Syndrome
Cardiovascular System Disease

  • Abnormality Of The Cardiovascular System

  • Cardiovascular Disease

  • Disease Of Subdivision Of Hemolymphoid System

  • Disorder Of Cardiovascular System

  • Cardiovascular Diseases
Huntington Disease

  • Huntington'S Disease

  • Huntington Chorea

  • Huntington'S Chorea

  • HD

  • Huntington Chronic Progressive Hereditary Chorea

  • Juvenile Huntington Disease

  • Chronic Progressive Chorea

  • Chronic Progressive Hereditary Chorea

  • Hc - [Huntington Chorea]

  • Hereditary Chorea

  • Progressive Hereditary Chorea
Cerebral Palsy

  • Infantile Cerebral Palsy

  • Mixed Cerebral Palsy

  • Palsy Cerebral

  • Palsy, Cerebral

  • Cerebral Palsy, Mixed
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
Short Syndrome

  • Short Stature, Hyperextensibility, Hernia, Ocular Depression, Rieger Anomaly, And Teething Delay

  • Aarskog-Ose-Pande Syndrome

  • Lipodystrophy, Partial, With Rieger Anomaly And Short Stature

  • Lipodystrophy-Rieger Anomaly-Diabetes Syndrome

  • Rieger Anomaly-Partial Lipodystrophy Syndrome

  • Partial Lipodystrophy With Rieger Anomaly And Short Stature

  • Short Stature, Hyperextensibility, Hernia, Ocular Depression, Rieger Anomaly And Teething Delay

  • Growth Retardation-Rieger Anomaly

  • Short Stature-Hyperextensibility-Rieger Anomaly-Teething Delay

  • SHORTS
Cataract 23, Multiple Types

  • Cataract 23

  • CTRCT23

  • Lamellar Cataract 23

  • Cataract 23, Multiple Types, With Or Without Microcornea

  • Isolated Microphthalmia With Cataract 4

  • Mcopct4

  • Cataract, Type 23

  • Microphthalmia, Isolated, With Cataract 4
Heart Disease

  • Heart Failure

  • Congenital Heart Disease

  • Heart Diseases

  • Congenital Heart Defects

  • Congenital Heart Defect

  • Heart Malformation

  • Congenital Anomaly Of Heart

  • Heart Defect

  • Heart-Congenital Defect

  • Congenital Heart Disorder

  • Heart Defects Congenital

  • Heart Defects, Congenital

  • Heart Defects

  • Heart Disease, Congenital

  • Disease, Heart, Congenital

  • Congestive Heart Failure
Pancreatic Colloid Cystadenoma

  • Mucinous Cystadenoma Of Pancreas
Chronic Wasting Disease

  • Wasting Disease, Chronic
Anthracosis

  • Black Lung

  • Coal Workers' Pneumoconiosis

  • Melanoedema

  • Black Lung Disease

  • Pneumoconiosis

  • Coal Miner'S Pneumoconiosis

  • Coal Workers' Lung

  • Coal Worker'S Pneumoconiosis

  • Coal Workers Pneumoconiosis

  • Coal Miners' Lung

  • Coal Miners' Pneumoconiosis

  • Coal Pneumoconiosis

  • Colliers' Anthracosis

  • Colliers' Lung

  • Lung Melanosis

  • Miners' Asthma

  • Miners' Lung

  • Pneumomelanosis

  • Cwp - [Coalworkers Pneumoconiosis]

  • Fibrosis Of Lung With Anthracosilicosis

  • Lung Fibrosis With Anthracosis

  • Miners' Pneumoconiosis

  • Carbon Lung

  • Coalworker Lung

  • Collier'S Asthma

  • Anthracosilicosis

  • Lung Anthracosis
Microvascular Complications Of Diabetes 5

  • Diabetic Retinopathy

  • Microvascular Complications Of Diabetes, Susceptibility To, 5

  • MVCD5

  • Retinopathy, Diabetic

  • Diabetic Nephropathy

  • Retinopathy, Diabetic, Susceptibility To

  • Retinal Abnormality - Diabetes-Related
Inclusion Body Myopathy With Paget Disease Of Bone And Frontotemporal Dementia

  • Ibmpfd

  • Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dementia

  • Pagetoid Amyotrophic Lateral Sclerosis

  • Pagetoid Neuroskeletal Syndrome

  • Inclusion Body Myopathy With Paget Disease Of Bone And/Or Frontotemporal Dementia

  • Inclusion Body Myopathy With Early-Onset Paget Disease Of Bone And/Or Frontotemporal Dementia

  • Multisystem Proteinopathy

  • Limb-Girdle Muscular Dystrophy With Paget Disease Of Bone

  • Inclusion Body Myopathy With Paget'S Disease Of Bone And Frontotemporal Dementia

  • Inclusion Body Myopathy With Early-Onset Paget Disease And Frontotemporal Dement

  • Lower Motor Neuron Degeneration With Paget-Like Bone Disease

  • Muscular Dystrophy, Limb-Girdle, With Paget Disease Of Bone

  • Myopathy, Inclusion Body, With Early-Onset Paget Disease And Frontotemporal Dementia
Chronic Kidney Disease

  • Chronic Renal Disease

  • Chronic Kidney Failure

  • Ckd

  • Chronic Renal Failure

  • Kidney Failure, Chronic

  • Chronic Renal Failure Syndrome

  • Crf

  • Renal Failure - Chronic

  • Renal Failure Chronic

  • Chronic Kidney Diseases

  • Chronic Kidney Disease Stage 5

  • Ckd - [Chronic Kidney Disease]

  • Crf - [Chronic Renal Failure]

  • Chronic Kidney Impairment

  • Chronic Renal Impairment

  • Chronic Kidney Shutdown

  • Chronic Hypoxic Kidney Failure

  • Chronic Kidney Collapse

  • Chronic Renal Insufficiency

  • Chronic Kidney Toxaemia

  • Chronic Kidney Hypofunction

  • Chronic Renal Suppression

  • Chronic Renal Failure, Stage 5

  • Ckd - [Chronic Kidney Disease] Stage 5

  • End Stage Kidney Failure

  • End Stage Renal Failure

  • End Stage Kidney Disease

  • End Stage Renal Disease

  • End Stage Chronic Renal Failure

  • Esrf - [End Stage Renal Failure]

  • Esrd - [End Stage Renal Diseases]

  • Egfr - [Estimated Glomerular Filtration Rate] < 15 Ml/Min/1.73m²
Autism Spectrum Disorder

  • Asd

  • Autism Spectrum Disorders

  • Autistic Continuum

  • Pervasive Developmental Disorder

  • Pervasive Development Disorder

  • Autistic Behavior

  • Autistic Disorder

  • Autistic

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Childhood Autism

  • Kanner Syndrome

  • Pervasive Developmental Delay Nos

  • Pervasive Developmental Disorder, Not Otherwise Specified
Malaria

  • Malaria, Susceptibility To

  • Malaria, Resistance To

  • Malaria, Cerebral

  • Cerebral Malaria

  • Malaria, Severe, Susceptibility To

  • Malaria, Severe, Resistance To

  • Malaria, Cerebral, Susceptibility To

  • Induced Malaria

  • Malaria, Vivax, Protection Against

  • Malaria, Severe

  • Malaria, Cerebral, Reduced Risk Of

  • Malaria, Protection Against

  • Resistance To Malaria Due To G6pd Deficiency

  • Malaria Due To G6pd Deficiency

  • Malarial Encephalitis

  • CM

  • Malaria Cerebral

  • Susceptibility To Malaria

  • Acute Pernicious Fever

  • Aestivo-Autumnal Fever

  • Aestivo Autumnal Malaria

  • Chagres Fever

  • Continued Malaria Fever

  • Estivo-Autumnal Fever

  • Estivo-Autumnal Malaria

  • Estivo-Autumnal Malarial Fever

  • Falciparum Fever

  • Malignant Tertian Fever

  • Malignant Tertian Malaria

  • Pernicious Intermittent Fever

  • Pernicious Malaria

  • Quotidian Malaria

  • Subtertian Fever

  • Subtertian Malaria Fever

  • Subtertian Malignant Tertian Malaria

  • Tropical Malaria

  • Algid Malaria

  • Bilious Haemoglobinuric Fever

  • Black Water Fever

  • Blackwater Fever

  • Malarial Blackwater Fever

  • Severe Malarial Falciparum

  • West African Fever

  • Malarial Haematinuria

  • Haemoglobinuric Fever

  • Haemoglobinuric Malaria

  • Severe Plasmodium Falciparum Malaria

  • Malarial Haemoglobinuria

  • Malarial Haematuria

  • Falciparum Malaria [Malignant Tertian]

  • Malaria Tropica

  • Malarial Shock

  • Chagres Virus Disease

  • Malignant Malaria

  • Mtm - [Malignant Tertian Malaria]

  • Tm -[Malignant Tertian Malaria]

  • Panama Fever

  • St - [Subtertian Malaria]

  • Malarial Quotidian

  • Benign Tertian Malaria

  • Tertian Ague

  • Vivax Fever

  • Plasmodium Vivax Malaria Nos

  • Btm - [Benign Tertian Malaria]

  • Bt - [Benign Tertian Malaria]

  • Vivax Malaria

  • Benign Tertian Vivax Malaria

  • Tertian Malaria

  • Quartan Malaria

  • Quartan Ague

  • Quartan Fever

  • Plasmodium Malariae Malaria Nos

  • Quartan Malarial

  • Malaria By Plasmodium Malariae

  • Malariae Malaria

  • Ovale Tertian Malaria

  • Plasmodium Ovale Fever

  • Malaria Fever By Plasmodium Ovale

  • Ovale Malaria

  • Malaria By Plasmodium Ovale

  • Malarial Ovale

  • Marsh Fever

  • Remittent Congestive Fever

  • Coastal Fever

  • Remittent Gastric Fever

  • Miasmatic Fever

  • Congestive Remittent Fever

  • Intermittent Fever

  • Jungle Fever

  • Paludism

  • Cameroon Fever

  • Ague

  • Corsican Fever

  • Intermittent Bilious Fever

  • Disease Due To Plasmodiidae

  • Malarial Fever

  • Plasmodiosis

  • Remittent Fever

  • Roman Fever

  • Malaria Fever Nos

  • Malaria Nos

  • Paludal Fever

  • Clinically Diagnosed Malaria

  • Clinically Diagnosed Malaria Without Parasitological Confirmation

  • Congestive Fever

  • Malarial Cachexia

  • Marsh Cachexia

  • Paludal Cachexia

  • Recurrent Malaria

  • Remittent Malaria
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]
Pick Disease Of Brain

  • Pick Disease

  • Pick'S Disease

  • Pick Disease Of The Brain

  • Lobar Atrophy Of Brain

  • Dementia With Lobar Atrophy And Neuronal Cytoplasmic Inclusions

  • Behavioral Variant Of Frontotemporal Dementia

  • Dementia In Pick'S Disease

  • Lobar Atrophy Of The Brain

  • Bvftd

  • Bv-Ftd

  • PIDB

  • Picks Disease
Neuroblastoma

  • Nb

  • Neuroblastoma, Susceptibility To

  • Neuroblastomas

  • Central Neuroblastoma
Pheochromocytoma

  • Pheochromocytoma, Susceptibility To

  • Phaeochromocytoma

  • Adrenal Gland Chromaffin Paraganglioma

  • Adrenal Gland Chromaffinoma

  • Adrenal Gland Paraganglioma

  • Adrenal Gland Pheochromocytoma

  • Chromaffin Paraganglioma Of The Adrenal Gland

  • Intraadrenal Paraganglioma

  • PCC

  • Chromaffin Cell Tumor

  • Medullary Chromaffinoma

  • Medullary Paraganglioma

  • Pheochromoblastoma

  • Pheochromocytomas

  • Chromaffin Cell Neoplasm

  • Pheochromocytoma, Malignant
Hereditary Ataxia

  • Sca

  • Spinocerebellar Ataxia

  • Ataxias Hereditary

  • Ataxias, Hereditary
Autosomal Dominant Cerebellar Ataxia

  • Spinocerebellar Ataxia

  • Adca

  • Pierre Marie Cerebellar Ataxia

  • Ataxia, Spinocerebellar

  • Sca

  • Autosomal Dominant Spinocerebellar Ataxia

  • Spinocerebellar Ataxias
Spastic Paraplegia 38, Autosomal Dominant

  • SPG38

  • Hereditary Spastic Paraplegia 38

  • Autosomal Dominant Spastic Paraplegia Type 38

  • Autosomal Dominant Spastic Paraplegia 38
Supranuclear Palsy, Progressive, 1

  • Progressive Supranuclear Palsy

  • Steele-Richardson-Olszewski Syndrome

  • Supranuclear Palsy, Progressive

  • Progressive Supranuclear Ophthalmoplegia

  • Psp

  • PSNP1

  • Familial Progressive Supranuclear Palsy

  • Richardson'S Syndrome

  • Psp Syndrome

  • Progressive Supranuclear Palsy 1

  • Supranuclear Palsy Progressive

  • Ophthalmoplegia, Supranuclear, Progressive

  • Steele-Richardson-Olszewksi Syndrome
Tetralogy Of Fallot

  • TOF

  • Fallot Tetralogy

  • Ventricular Septal Defect With Pulmonary Stenosis Or Atresia, Dextraposition Of Aorta, And Hypertrophy Of Right Ventricle

  • Tetrad Of Fallot

  • Fallot Tetrad

  • Fallot Disease

  • Fallot Complex

  • Subpulmonic Stenosis, Ventricular Septal Defect, Overriding Aorta, And Right Ventricular Hypertrophy

  • Interventricular Septal Defect With Dextroposition Of Aorta, Pulmonary Stenosis And Hypertrophy Of Right Ventricle

  • Interventricular Septal Defect, In Tetralogy Of Fallot

  • Ventricular Septal Defect With Obstructed Right Ventricular Outflow

  • Tof - [Tetralogy Of Fallot]

  • Pulmonary Atresia With Ventricular Septal Defect [Fallot Type]

  • Pulmonary Atresia, Ventricular Septal Defect And Mapcas

  • Pulmonary Atresia With Ventricular Septal Defect And Systemic-To-Pulmonary Collateral Arteries [Fallot Type]
Cerebellar Disease

  • Cerebellar Diseases

  • Cerebellar Dysfunction

  • Cerebellar Abnormality

  • Cerebellar Disorders
Alzheimer Disease 9

  • AD9

  • Alzheimer'S Disease 9

  • Alzheimer Disease 9, Susceptibility To

  • Alzheimer Disease 9, Late-Onset

  • Alzheimer'S Disease 9, Late Onset

  • {Alzheimer Disease 9, Susceptibility To}
Neuromuscular Disease

  • Neuromuscular Diseases

  • Neuromuscular Disorders

  • Neuromuscular Disorder
Scoliosis
Spinal Muscular Atrophy, Type I

  • Werdnig-Hoffmann Disease

  • SMA1

  • Spinal Muscular Atrophy 1

  • Sma I

  • Sma, Infantile Acute Form

  • Muscular Atrophy, Infantile

  • Spinal Muscular Atrophy-1

  • Hmn Proximal Type I

  • Infantile Muscular Atrophy

  • Proximal Spinal Muscular Atrophy Type 1

  • Sma Type 1

  • Sma Type I

  • Sma-I

  • Hereditary Motor Neuropathy Proximal Type I

  • Progressive Muscular Atrophy Of Infancy

  • Proximal Spinal Muscular Atrophy, Type 1

  • Werdnig Hoffmann Disease

  • Infantile Spinal Muscular Atrophy

  • Infantile-Onset Spinal Muscular Atrophy

  • Proximal Hereditary Motor Neuropathy Type I

  • Sma Infantile Acute Form

  • Spinal Muscular Atrophy Type I

  • Werdnig-Hoffman Disease

  • Atrophy, Muscular, Spinal, Type 1
Autism

  • Autistic Disorder

  • Autism Susceptibility 1

  • Childhood Autism

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Kanner'S Syndrome

  • Autistic
Movement Disease

  • Movement Disorders

  • Movement Disorder
Giant Axonal Neuropathy 2
Choreatic Disease

  • Chorea

  • Hereditary Chorea
Schizophrenia

  • SCZD

  • Schizophrenia With Or Without An Affective Disorder

  • Schizophrenia 12

  • Schizophrenia, Susceptibility To

  • Schizophrenia-1

  • Dementia Praecox

  • Schizophrenia 1
Hereditary Spastic Paraplegia

  • Familial Spastic Paraplegia

  • Hereditary Spastic Paraparesis

  • Strumpell-Lorrain Disease

  • Familial Spastic Paraparesis

  • Hsp

  • Spg

  • Strümpell-Lorrain Disease

  • Spastic Paraplegia, Hereditary

  • French Settlement Disease

  • Strumpell-Lorrain Syndrome

  • Fsp

  • Spastic Paraplegia, Familial

  • Spastic Paraplegia Hereditary

  • Spastic Paraplegia 3, Autosomal Dominant

  • Spastic Paraparesis

  • Hereditary Spastic Paralysis

  • Familial Spastic Paralysis

  • Hereditary Spastic Ataxia
Respiratory Failure

  • Acute Respiratory Failure

  • Chronic Respiratory Failure

  • Respiratory Insufficiency

  • Acute-On-Chronic Respiratory Failure

  • Respiratory Disease

  • Acute And Chronic Respiratory Failure

  • Respiratory Insufficiency/Failure

  • Chronic Respiratory Disease

  • Pulmonary Valve Insufficiency

  • Chronic Disease Of Respiratory System

  • Respiration Disorders

  • Respiratory Tract Diseases

  • Lung Failure Nos

  • Pulmonary Failure

  • Arf - [Acute Respiratory Failure]

  • Acute Respiratory Insufficiency

  • Acute Pulmonary Insufficiency

  • Acute Respiration Failure

  • Chronic Respiration Failure
Peripheral Nervous System Disease

  • Peripheral Neuropathy

  • Peripheral Nerve Disease

  • Peripheral Nerve Disorders

  • Neuropathy, Peripheral

  • Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation
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
Nervous System Disease

  • Abnormality Of The Nervous System

  • Nervous System Diseases

  • Nervous System Disorder
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
Myopathy

  • Muscular Diseases

  • Myopathies
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
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

Related Agents

  • Approval
  • Clinical Phase
  • Pre-clinical Phase

Approval

Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Rare Diseases
HY-132580 Tofersen Inhibitor 96.53% Unkown

Clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name Effect
Purity Phase
HY-16074 ATN-224 98.0% Phase 2

Pre-clinical Phase

Bioactive Molecules (26)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-W115718 Cuprizone 99.61% Unkown
HY-115445 LCS-1 99.81% Unkown
HY-132580A Tofersen sodium Inhibitor 97.55% Unkown
HY-153019 NUCC-0000323 Inhibitor 99.86% Unkown
HY-173025 Nurr1 agonist 12 Agonist 99.62% Unkown
HY-148901 CMB-087229 Inhibitor 98.05% Unkown
HY-E70377 Cu/Zn Superoxide dismutase / Unkown
HY-123982 SOD1-Derlin-1 inhibitor-2 Inhibitor 99.86% Unkown
HY-138131 SOD1-Derlin-1 inhibitor-1 Inhibitor 99.93% Unkown
HY-RS13559 SOD1 Human Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-W073128 Perfluorotetradecanoic acid 98.0% Unkown
HY-145294 ROCK2-IN-5 Inhibitor / Unkown
HY-163772 Fraxinellone analog 1 Activator / Unkown
HY-172152 MP-010 / Unkown
HY-176827 SOD1-IN-1 Inhibitor / Unkown
HY-179533 SOD1-aggregation-IN-1 Inhibitor / Unkown
HY-182304 CLR01 sodium Inhibitor / Unkown
HY-182446 SRI-22818 Activator / Unkown
HY-182648 K811 Inhibitor / Unkown
HY-184165 F2F-202 Inhibitor / Unkown
HY-P10627 SOD1 (147-153) human / Unkown
HY-132580S Tofersen-d27 Inhibitor / Unkown
HY-161612 Mycosporine 2 glycine Inhibitor / Unkown
HY-183933 K812 Inhibitor / Unkown
HY-RS16926 Sod1 Mouse Pre-designed siRNA Set A Pre-designed Set / Unkown
HY-RS23369 Sod1 Rat Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Canis familiaris SOD1 VGNC VGNC:46653
Rattus norvegicus SOD1 RGD RGD:3731
Macaca mulatta SOD1 VGNC VGNC:77687
Mus musculus SOD1 MGD MGI:98351
Others SOD1 NCBI