CALR - calreticulin Gene

Also Known as RO; CRT; SSA; cC1qR; HEL-S-99n

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 811

About CALR

Cytogenetic location: 19p13.13 Genomic coordinates (GRCh38): 19:12,938,609-12,944,489 (from NCBI)

This gene has 8 transcripts (splice variants), 195 orthologues, 3 paralogues and is associated with 73 phenotypes. Ubiquitous expression in thyroid (RPKM 564.2), placenta (RPKM 291.4) and 24 other tissues.

Summary

Calreticulin is a highly conserved chaperone protein which resides primarily in the endoplasmic reticulum, and is involved in a variety of cellular processes, among them, cell adhesion. Additionally, it functions in protein folding quality control and calcium homeostasis. Calreticulin is also found in the nucleus, suggesting that it may have a role in transcription regulation. Systemic lupus erythematosus is associated with increased autoantibody titers against calreticulin. Recurrent mutations in calreticulin have been linked to various neoplasms, including the myeloproliferative type.[provided by RefSeq, May 2020]

CALR Products (2)

mRNA Protein Name
NM_004343.4 NP_004334.1 calreticulin precursor
NM_004343.4 NP_004334.1 calreticulin precursor
Molecular Function GO Annotation Evidence References Source
enables calcium ion binding IDA
IDA: Inferred from direct assay
21590275 GOA
enables calcium ion binding IMP
IMP: Inferred from mutant phenotype
21705382 GOA
enables complement component C1q complex binding IPI
IPI: Inferred from physical interaction
9922153 GOA
enables integrin binding IPI
IPI: Inferred from physical interaction
1911778 GOA
enables mRNA binding IDA
IDA: Inferred from direct assay
14726956 GOA
enables molecular sequestering activity IDA
IDA: Inferred from direct assay
35948544 GOA
enables nuclear androgen receptor binding IDA
IDA: Inferred from direct assay
8107809 GOA
enables nuclear export signal receptor activity IDA
IDA: Inferred from direct assay
11149926 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
9640257 GOA
enables ubiquitin protein ligase binding IPI
IPI: Inferred from physical interaction
8666824 GOA
Biological Process GO Annotation Evidence References Source
involved in cellular senescence IGI
IGI: Inferred from genetic interaction
14726956 GOA
involved in negative regulation of DNA-templated transcription IDA
IDA: Inferred from direct assay
8107809 GOA
involved in negative regulation of intracellular steroid hormone receptor signaling pathway IDA
IDA: Inferred from direct assay
8107809 GOA
involved in negative regulation of neuron differentiation IDA
IDA: Inferred from direct assay
8107809 GOA
involved in negative regulation of retinoic acid receptor signaling pathway IDA
IDA: Inferred from direct assay
8107809 GOA
involved in negative regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
8107809 GOA
involved in negative regulation of translation IDA
IDA: Inferred from direct assay
14726956 GOA
involved in negative regulation of trophoblast cell migration IMP
IMP: Inferred from mutant phenotype
22377355 GOA
involved in peptide antigen assembly with MHC class I protein complex IDA
IDA: Inferred from direct assay
35948544 GOA
acts upstream of positive regulation of cell cycle IGI
IGI: Inferred from genetic interaction
14726956 GOA
involved in positive regulation of cell population proliferation IGI
IGI: Inferred from genetic interaction
14726956 GOA
involved in positive regulation of dendritic cell chemotaxis IMP
IMP: Inferred from mutant phenotype
16140380 GOA
involved in positive regulation of endothelial cell migration IMP
IMP: Inferred from mutant phenotype
22377355 GOA
involved in positive regulation of substrate adhesion-dependent cell spreading IMP
IMP: Inferred from mutant phenotype
11859136 GOA
involved in protein export from nucleus IDA
IDA: Inferred from direct assay
11149926 GOA
involved in protein localization to nucleus IDA
IDA: Inferred from direct assay
15998798 GOA
Cellular Component GO Annotation Evidence References Source
part of MHC class I peptide loading complex IDA
IDA: Inferred from direct assay
21263072 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
1911778 GOA
located in cytosol IDA
IDA: Inferred from direct assay
11149926 GOA
located in endoplasmic reticulum IDA
IDA: Inferred from direct assay
23011799 GOA
located in endoplasmic reticulum lumen IDA
IDA: Inferred from direct assay
11149926 GOA
located in extracellular space IMP
IMP: Inferred from mutant phenotype
22377355 GOA
located in membrane IDA
IDA: Inferred from direct assay
22572157 GOA
located in nuclear envelope IDA
IDA: Inferred from direct assay
21590275 GOA
located in nucleus IDA
IDA: Inferred from direct assay
8107809 GOA
located in perinuclear region of cytoplasm IDA
IDA: Inferred from direct assay
1911778 GOA
located in ribosome IDA
IDA: Inferred from direct assay
14726956 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

CALR Protein Structure

Calreticulin

Calreticulin: cl02828 (22 - 331)

  • 0
  • 100
  • 200
  • 300
  • 417 a.a.
Protein Preferred Names Protein Names

calreticulin

  • CRP55

CALR Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
CALR P27797 KIAA1683 Homo sapiens A0JP07 32814053
Intra
CALR P27797 KIAA1683 Homo sapiens A0JP07 32814053
Intra
CALR P27797 KIAA1683 Homo sapiens A0JP07 32814053
Intra
CALR P27797 CAMTA2 Homo sapiens O94983-5 32814053
Intra
CALR P27797 CAMTA2 Homo sapiens O94983-5 32814053
Intra
CALR P27797 CAMTA2 Homo sapiens O94983-5 32814053
Intra
CALR P27797 DRC7 Homo sapiens Q8IY82 32814053
Intra
CALR P27797 DRC7 Homo sapiens Q8IY82 32814053
Intra
CALR P27797 DRC7 Homo sapiens Q8IY82 32814053
Intra
CALR P27797 EVA1B Homo sapiens Q9NVM1 32814053
Intra
CALR P27797 EVA1B Homo sapiens Q9NVM1 32814053
Intra
CALR P27797 EVA1B Homo sapiens Q9NVM1 32814053
Intra
CALR P27797 TPX2 Homo sapiens Q9ULW0 32814053
Intra
CALR P27797 TPX2 Homo sapiens Q9ULW0 32814053
Intra
CALR P27797 TPX2 Homo sapiens Q9ULW0 32814053
Intra
CALR P27797 LGALS1 Homo sapiens P09382 32814053
Intra
CALR P27797 LGALS1 Homo sapiens P09382 32814053
Intra
CALR P27797 LGALS1 Homo sapiens P09382 32814053
Intra
CALR P27797 HUWE1 Homo sapiens Q7Z6Z7-2 32814053
Intra
CALR P27797 HUWE1 Homo sapiens Q7Z6Z7-2 32814053
Intra
CALR P27797 HUWE1 Homo sapiens Q7Z6Z7-2 32814053
Intra
CALR P27797 SP6 Homo sapiens Q3SY56 32814053
Intra
CALR P27797 SP6 Homo sapiens Q3SY56 32814053
Intra
CALR P27797 SP6 Homo sapiens Q3SY56 32814053
Intra
CALR P27797 EPCAM Homo sapiens P16422 32814053
Intra
CALR P27797 EPCAM Homo sapiens P16422 32814053
Intra
CALR P27797 EPCAM Homo sapiens P16422 32814053
Intra
CALR P27797 LEG1 Homo sapiens Q6P5S2 32814053
Intra
CALR P27797 LEG1 Homo sapiens Q6P5S2 32814053
Intra
CALR P27797 LEG1 Homo sapiens Q6P5S2 32814053
Intra
CALR P27797 NEK6 Homo sapiens Q9HC98-4 32814053
Intra
CALR P27797 NEK6 Homo sapiens Q9HC98-4 32814053
Intra
CALR P27797 NEK6 Homo sapiens Q9HC98-4 32814053
Intra
CALR P27797 TNMD Homo sapiens Q9H2S6-2 32814053
Intra
CALR P27797 TNMD Homo sapiens Q9H2S6-2 32814053
Intra
CALR P27797 TNMD Homo sapiens Q9H2S6-2 32814053
Intra
CALR P27797 LGALS8 Homo sapiens O00214-2 32814053
Intra
CALR P27797 LGALS8 Homo sapiens O00214-2 32814053
Intra
CALR P27797 LGALS8 Homo sapiens O00214-2 32814053
Intra
CALR P27797 NFATC2IP Homo sapiens Q8NCF5-2 32814053
Intra
CALR P27797 NFATC2IP Homo sapiens Q8NCF5-2 32814053
Intra
CALR P27797 NFATC2IP Homo sapiens Q8NCF5-2 32814053
Intra
CALR P27797 TRNAU1AP Homo sapiens Q9NX07 32814053
Intra
CALR P27797 TRNAU1AP Homo sapiens Q9NX07 32814053
Intra
CALR P27797 TRNAU1AP Homo sapiens Q9NX07 32814053
Intra
CALR P27797 SPATA17 Homo sapiens Q96L03 32814053
Intra
CALR P27797 SPATA17 Homo sapiens Q96L03 32814053
Intra
CALR P27797 SPATA17 Homo sapiens Q96L03 32814053
Intra
CALR P27797 TAF1B Homo sapiens Q53T94 32296183
Intra
CALR P27797 TAF1B Homo sapiens Q53T94 32296183
Intra
CALR P27797 TAF1B Homo sapiens Q53T94 32296183
Intra
CALR P27797 HSD3B1 Homo sapiens P14060 32814053
Intra
CALR P27797 HSD3B1 Homo sapiens P14060 32814053
Intra
CALR P27797 HSD3B1 Homo sapiens P14060 32814053
Intra
CALR P27797 GSC2 Homo sapiens O15499 32296183
Intra
CALR P27797 GSC2 Homo sapiens O15499 32296183
Intra
CALR P27797 DNASE1L1 Homo sapiens P49184 32814053
Intra
CALR P27797 DNASE1L1 Homo sapiens P49184 32814053
Intra
CALR P27797 DNASE1L1 Homo sapiens P49184 32814053
Intra
CALR P27797 FAHD2A Homo sapiens Q96GK7 32814053
Intra
CALR P27797 FAHD2A Homo sapiens Q96GK7 32814053
Intra
CALR P27797 FAHD2A Homo sapiens Q96GK7 32814053
Intra
CALR P27797 CRELD2 Homo sapiens Q6UXH1-2 32814053
Intra
CALR P27797 CRELD2 Homo sapiens Q6UXH1-2 32814053
Intra
CALR P27797 CRELD2 Homo sapiens Q6UXH1-2 32814053
Intra
CALR P27797 q9bq29_human Homo sapiens Q9BQ29 32814053
Intra
CALR P27797 q9bq29_human Homo sapiens Q9BQ29 32814053
Intra
CALR P27797 q9bq29_human Homo sapiens Q9BQ29 32814053
Intra
CALR P27797 USP12 Homo sapiens O75317 32814053
Intra
CALR P27797 USP12 Homo sapiens O75317 32814053
Intra
CALR P27797 USP12 Homo sapiens O75317 32814053
Intra
CALR P27797 THBS3 Homo sapiens P49746 32814053
Intra
CALR P27797 THBS3 Homo sapiens P49746 32814053
Intra
CALR P27797 THBS3 Homo sapiens P49746 32814053
Intra
CALR P27797 POC1A Homo sapiens Q8NBT0 32814053
Intra
CALR P27797 POC1A Homo sapiens Q8NBT0 32814053
Intra
CALR P27797 POC1A Homo sapiens Q8NBT0 32814053
Intra
CALR P27797 ISY1 Homo sapiens Q9ULR0 32814053
Intra
CALR P27797 ISY1 Homo sapiens Q9ULR0 32814053
Intra
CALR P27797 ISY1 Homo sapiens Q9ULR0 32814053
Intra
CALR P27797 ZHX1-C8orf76 Homo sapiens Q96EF9 32814053
Intra
CALR P27797 ZHX1-C8orf76 Homo sapiens Q96EF9 32814053
Intra
CALR P27797 ZHX1-C8orf76 Homo sapiens Q96EF9 32814053
Intra
CALR P27797 TAFAZZIN Homo sapiens F6Y2X3 32814053
Intra
CALR P27797 TAFAZZIN Homo sapiens F6Y2X3 32814053
Intra
CALR P27797 TAFAZZIN Homo sapiens F6Y2X3 32814053
Intra
CALR P27797 U2AF1 Homo sapiens Q7Z780 32814053
Intra
CALR P27797 U2AF1 Homo sapiens Q7Z780 32814053
Intra
CALR P27797 U2AF1 Homo sapiens Q7Z780 32814053
Intra
CALR P27797 TMX3 Homo sapiens Q96JJ7-2 32814053
Intra
CALR P27797 TMX3 Homo sapiens Q96JJ7-2 32814053
Intra
CALR P27797 TMX3 Homo sapiens Q96JJ7-2 32814053
Intra
CALR P27797 NXPE1 Homo sapiens Q8N323 32814053
Intra
CALR P27797 NXPE1 Homo sapiens Q8N323 32814053
Intra
CALR P27797 NXPE1 Homo sapiens Q8N323 32814053
Intra
CALR P27797 MGC39372 Homo sapiens Q8TB02 32814053
Intra
CALR P27797 MGC39372 Homo sapiens Q8TB02 32814053
Intra
CALR P27797 MGC39372 Homo sapiens Q8TB02 32814053
Intra
CALR P27797 PRAM1 Homo sapiens Q96QH2 32814053
Intra
CALR P27797 PRAM1 Homo sapiens Q96QH2 32814053
Intra
CALR P27797 PRAM1 Homo sapiens Q96QH2 32814053
Intra
CALR P27797 PPEF1 Homo sapiens O14829 32814053
Intra
CALR P27797 PPEF1 Homo sapiens O14829 32814053
Intra
CALR P27797 PPEF1 Homo sapiens O14829 32814053
Intra
CALR P27797 PYGO1 Homo sapiens Q9Y3Y4 32814053
Intra
CALR P27797 PYGO1 Homo sapiens Q9Y3Y4 32814053
Intra
CALR P27797 PYGO1 Homo sapiens Q9Y3Y4 32814053
Intra
CALR P27797 MYNN Homo sapiens Q9NPC7 32814053
Intra
CALR P27797 MYNN Homo sapiens Q9NPC7 32814053
Intra
CALR P27797 MYNN Homo sapiens Q9NPC7 32814053
Intra
CALR P27797 TUBB Homo sapiens P07437 32814053
Intra
CALR P27797 TUBB Homo sapiens P07437 32814053
Intra
CALR P27797 TUBB Homo sapiens P07437 32814053
Intra
CALR P27797 HSPB1 Homo sapiens P04792 25277244
Intra
CALR P27797 PSMD2 Homo sapiens Q13200 32814053
Intra
CALR P27797 PSMD2 Homo sapiens Q13200 32814053
Intra
CALR P27797 PSMD2 Homo sapiens Q13200 32814053
Intra
CALR P27797 RAP1B Homo sapiens P61224 32814053
Intra
CALR P27797 RAP1B Homo sapiens P61224 32814053
Intra
CALR P27797 RAP1B Homo sapiens P61224 32814053
Intra
CALR P27797 SMARCB1 Homo sapiens Q12824
Y2H
21900206
Intra
CALR P27797 SLC25A11 Homo sapiens Q02978 32814053
Intra
CALR P27797 SLC25A11 Homo sapiens Q02978 32814053
Intra
CALR P27797 SLC25A11 Homo sapiens Q02978 32814053
Intra
CALR P27797 HLA-DRB3 Homo sapiens P79483 32814053
Intra
CALR P27797 HLA-DRB3 Homo sapiens P79483 32814053
Intra
CALR P27797 HLA-DRB3 Homo sapiens P79483 32814053
Intra
CALR P27797 EGFL8 Homo sapiens Q99944 32814053
Intra
CALR P27797 EGFL8 Homo sapiens Q99944 32814053
Intra
CALR P27797 EGFL8 Homo sapiens Q99944 32814053
Intra
CALR P27797 RAB3C Homo sapiens Q96E17 32814053
Intra
CALR P27797 RAB3C Homo sapiens Q96E17 32814053
Intra
CALR P27797 RAB3C Homo sapiens Q96E17 32814053
Intra
CALR P27797 PIAS4 Homo sapiens Q8N2W9 32814053
Intra
CALR P27797 PIAS4 Homo sapiens Q8N2W9 32814053
Intra
CALR P27797 PIAS4 Homo sapiens Q8N2W9 32814053
Intra
CALR P27797 MAGEA2 Homo sapiens P43356 32814053
Intra
CALR P27797 MAGEA2 Homo sapiens P43356 32814053
Intra
CALR P27797 MAGEA2 Homo sapiens P43356 32814053
Intra
CALR P27797 NLRP3 Homo sapiens Q96P20 32814053
Intra
CALR P27797 NLRP3 Homo sapiens Q96P20 32814053
Intra
CALR P27797 NLRP3 Homo sapiens Q96P20 32814053
Intra
CALR P27797 SPRED2 Homo sapiens Q7Z698 32814053
Intra
CALR P27797 SPRED2 Homo sapiens Q7Z698 32814053
Intra
CALR P27797 SPRED2 Homo sapiens Q7Z698 32814053
Intra
CALR P27797 PSAT1 Homo sapiens Q9Y617 32814053
Intra
CALR P27797 PSAT1 Homo sapiens Q9Y617 32814053
Intra
CALR P27797 PSAT1 Homo sapiens Q9Y617 32814053
Intra
CALR P27797 GABARAP Homo sapiens O95166
SPR
19154346
Intra
CALR P27797 RBM5 Homo sapiens P52756 32814053
Intra
CALR P27797 RBM5 Homo sapiens P52756 32814053
Intra
CALR P27797 RBM5 Homo sapiens P52756 32814053
Intra
CALR P27797 GNAO1 Homo sapiens P09471 32814053
Intra
CALR P27797 GNAO1 Homo sapiens P09471 32814053
Intra
CALR P27797 GNAO1 Homo sapiens P09471 32814053
Intra
CALR P27797 IDH1 Homo sapiens O75874 32814053
Intra
CALR P27797 IDH1 Homo sapiens O75874 32814053
Intra
CALR P27797 IDH1 Homo sapiens O75874 32814053
Intra
CALR P27797 RAB31 Homo sapiens Q13636 32814053
Intra
CALR P27797 RAB31 Homo sapiens Q13636 32814053
Intra
CALR P27797 RAB31 Homo sapiens Q13636 32814053
Intra
CALR P27797 RBM17 Homo sapiens Q96I25 32814053
Intra
CALR P27797 RBM17 Homo sapiens Q96I25 32814053
Intra
CALR P27797 RBM17 Homo sapiens Q96I25 32814053
Intra
CALR P27797 THAP7 Homo sapiens Q9BT49 32814053
Intra
CALR P27797 THAP7 Homo sapiens Q9BT49 32814053
Intra
CALR P27797 THAP7 Homo sapiens Q9BT49 32814053
Intra
CALR P27797 CNOT3 Homo sapiens O75175 32814053
Intra
CALR P27797 CNOT3 Homo sapiens O75175 32814053
Intra
CALR P27797 CNOT3 Homo sapiens O75175 32814053
Intra
CALR P27797 TDO2 Homo sapiens P48775 32814053
Intra
CALR P27797 TDO2 Homo sapiens P48775 32814053
Intra
CALR P27797 TDO2 Homo sapiens P48775 32814053
Intra
CALR P27797 PSMC4 Homo sapiens P43686 32814053
Intra
CALR P27797 PSMC4 Homo sapiens P43686 32814053
Intra
CALR P27797 PSMC4 Homo sapiens P43686 32814053
Intra
CALR P27797 SGTB Homo sapiens Q96EQ0 32296183
Intra
CALR P27797 SGTB Homo sapiens Q96EQ0 32296183
Intra
CALR P27797 SGTB Homo sapiens Q96EQ0 32296183
Intra
CALR P27797 MFI Homo sapiens Q8NCR3 32814053
Intra
CALR P27797 MFI Homo sapiens Q8NCR3 32814053
Intra
CALR P27797 MFI Homo sapiens Q8NCR3 32814053
Intra
CALR P27797 TAP1 Homo sapiens Q03518 17055437
Intra
CALR P27797 C1orf216 Homo sapiens Q8TAB5 32814053
Intra
CALR P27797 C1orf216 Homo sapiens Q8TAB5 32814053
Intra
CALR P27797 C1orf216 Homo sapiens Q8TAB5 32814053
Intra
CALR P27797 GJA5 Homo sapiens P36382 32814053
Intra
CALR P27797 GJA5 Homo sapiens P36382 32814053
Intra
CALR P27797 GJA5 Homo sapiens P36382 32814053
Intra
CALR P27797 APP Homo sapiens P05067
PLA
25241761
Intra
CALR P27797 MMAB Homo sapiens Q96EY8 32814053
Intra
CALR P27797 MMAB Homo sapiens Q96EY8 32814053
Intra
CALR P27797 MMAB Homo sapiens Q96EY8 32814053
Intra
CALR P27797 KLRC1 Homo sapiens P26715 32814053
Intra
CALR P27797 KLRC1 Homo sapiens P26715 32814053
Intra
CALR P27797 KLRC1 Homo sapiens P26715 32814053
Intra
CALR P27797 MYBPHL Homo sapiens A2RUH7 32814053
Intra
CALR P27797 MYBPHL Homo sapiens A2RUH7 32814053
Intra
CALR P27797 MYBPHL Homo sapiens A2RUH7 32814053
Intra
CALR P27797 FUT2 Homo sapiens Q10981 32814053
Intra
CALR P27797 FUT2 Homo sapiens Q10981 32814053
Intra
CALR P27797 FUT2 Homo sapiens Q10981 32814053
Intra
CALR P27797 TPGS2 Homo sapiens Q68CL5-3 32814053
Intra
CALR P27797 TPGS2 Homo sapiens Q68CL5-3 32814053
Intra
CALR P27797 TPGS2 Homo sapiens Q68CL5-3 32814053
Intra
CALR P27797 PABIR3 Homo sapiens Q6P4D5-2 32814053
Intra
CALR P27797 PABIR3 Homo sapiens Q6P4D5-2 32814053
Intra
CALR P27797 PABIR3 Homo sapiens Q6P4D5-2 32814053
Intra
CALR P27797 RASSF2 Homo sapiens P50749 32814053
Intra
CALR P27797 RASSF2 Homo sapiens P50749 32814053
Intra
CALR P27797 RASSF2 Homo sapiens P50749 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Recombinant CALR Proteins

Cat. No. Product Name Accession Purity
HY-P72111 Calreticulin/CALR Protein, Human (His) P27797 (E18-L417) ≥ 90%, as determined by reducing SDS-PAGE.

CALR Antibodies

Cat. No. Product Name Application Reactivity
HY-P80043 Calreticulin Antibody (YA571) WB, ICC/IF, IHC-P, FC, IP Human, Mouse
HY-P84229 Calreticulin Antibody (YA3926) WB, IHC-P, FC, ELISA Human, Mouse, Rat
HY-P84229A Calreticulin Antibody (YA3926)(PBS only) WB, IHC-P, FC, ELISA Human, Mouse, Rat
HY-P85073 Calreticulin Antibody (YA4765) WB, IHC-P, ICC/IF, ELISA Human, Mouse
HY-P86567 Calreticulin Antibody (YA6259) WB, IHC-P, ICC/IF, IP, ELISA Human, Mouse, Rat

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  • Megakaryocytic Myelosclerosis

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  • Chronic Idiopathic Myelofibrosis

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Thrombocythemia 1
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Essential Thrombocythemia
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Budd-Chiari Syndrome
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Rubella
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Polycythemia Vera
  • PV

  • Polycythemia Rubra Vera

  • Prv

  • Osler-Vaquez Disease

  • Chronic Erythremia

  • Polycythaemia Rubra Vera

  • Primary Polycythemia

  • Vaquez Disease

  • Polycythemia Vera, Somatic

  • Osler-Vaquez Syndrome

  • Proliferative Polycythaemia

  • Polycythemia Ruba Vera

  • Acquired Primary Erythrocytosis

  • Heilmeyer-Schoner Disease

  • Vaquez Osler Disease

  • Primary Polycythaemia

Polycythemia
  • Erythrocythemia

  • Polycythemia Vera

  • Polycythaemia Due To High Altitude

Halothane Hepatitis
  • Hepatitis Halothane

Lupus Erythematosus
  • Lupus

  • Lupus Vulgaris

  • Lupus Erythematosus, Discoid

  • Lupus Erythematosus, Systemic

  • Subacute Cutaneous Lupus

  • Le - [Lupus Erythematosus]

Third-Degree Atrioventricular Block
  • Third Degree Atrioventricular Block

  • Complete Atrioventricular Block

  • Complete Av Block

  • Third-Degree Block

  • Complete Atrioventricular Heart Block

  • Complete Heart Block

  • Third Degree Atrioventricular Heart Block

  • Third Degree Heart Block

  • Complete Heart Block Nos

  • Chb - [Complete Heart Block]

  • Idioventricular Rhythm

  • Av - [Atrioventricular] Block, Complete

Sjogren Syndrome
  • Sicca Syndrome

  • Sjogren'S Syndrome

  • Sjögren Syndrome

  • Sjogren-Gougerot Syndrome

  • Keratoconjunctivitis Sicca

  • Sjögren'S Syndrome

  • Xerodermosteosis

  • Dacryosialoadenopathia Atrophicans

  • Gougerot-Houwer-Sjogren Syndrome

  • Gougerot-Sjogren Syndrome

  • Keratoconjunctivitis Sicca-Xerostomia

  • Secreto-Inhibitor-Xerodermostenosis

  • Primary Sjogren Syndrome

  • Primary Sjogren-Gougerot Syndrome

  • Sjogrens Syndrome Primary

  • Sjogrens Syndrome

  • Dry Eye Syndromes

Myelophthisic Anemia
  • Myelophthisis

  • Anemia Leukoerythroblastic

  • Anemia, Leukoerythroblastic

  • Leukoerythroblastosis

  • Anemia, Myelophthisic

  • Leukoerythroblastic Anemia

Myeloperoxidase Deficiency
  • Mpo Deficiency

  • MPOD

Thrombocytosis
  • Thrombocythaemia

Influenza
  • Flu

  • Influenza With Non-Respiratory Manifestation

  • Influenza With Other Manifestations

  • Influenza, Human

  • Influenza, Susceptibility To

  • Seasonal Influenza, Virus Identified

Catecholaminergic Polymorphic Ventricular Tachycardia
  • Cpvt

  • Catecholamine-Induced Polymorphic Ventricular Tachycardia

  • Familial Polymorphic Ventricular Tachycardia

  • Malignant Paroxysmal Ventricular Tachycardia

  • Multifocal Ventricular Premature Beats

  • Stress-Induced Polymorphic Ventricular Tachycardia

  • Bidirectional Tachycardia Induced By Catecholamine

  • Double Tachycardia Induced By Catecholamines

  • Polymorphic Catecholergic Ventricular Tachycardia

  • Syncopal Paroxysmal Tachycardia

  • Bidirectional Tachycardia Induced By Catecholamines

  • Fpvt

  • Bidirectional Ventricular Tachycardia Induced By Catecholamine

  • Polymorphic Ventricular Tachycardia Induced By Catecholamines

  • Ventricular Tachycardia, Catecholaminergic Polymorphic

  • Ventricular Tachycardia, Catecholaminergic Polymorphic, 1

  • Familial Ventricular Tachycardia

  • Multifocal Pvcs

  • Multifocal Premature Ventricular Beats

Onchocerciasis
  • Infection By Onchocerca Volvulus

  • River Blindness

  • Onchocerca Volvulus Infection

  • Volvulosis

  • Robles' Disease

  • Onchocerciasis, Ocular

  • Robles Disease

  • Onchocercosis

  • Blinding Filariasis

  • Robles

  • Onchocerca Infestation

  • Craw-Craw

Myeloid Leukemia
  • Myeloid Leukaemia

  • Leukaemia Myelogenous

  • Leukemia Myelogenous

  • Myeloid Granulocytic Leukaemia

  • Myeloid Granulocytic Leukemia

  • Non-Lymphocytic Leukemia

  • Leukemia, Myeloid

  • Granulocytic Leukaemia

  • Myelogenous Leukaemia

  • Myeloid Leukaemia, Unspecified, Without Mention Of Remission

Subacute Cutaneous Lupus Erythematosus
  • Lupus Erythematosus Cutaneous Subacute

  • Lupus Erythematosus, Subacute Cutaneous

  • Sacle - [Subacute Cutaneous Lupus Erythematosus]

  • Scle - [Subacute Cutaneous Lupus Erythematosus]

Systemic Lupus Erythematosus
  • Lupus Nephritis

  • SLE

  • Disseminated Lupus Erythematosus

  • Systemic Lupus Erythematosus, Susceptibility To

  • Lupus Erythematosus, Systemic

  • Lupus Nephritis, Susceptibility To

  • Libman-Sacks Disease

  • Systemic Lupus Erythematosus Susceptibility To

  • Sle - Lupus Erythematosus, Systemic

  • Le Syndrome

  • Lupus

  • Lupus Erythematosus Systemic

  • Lupus Erythematosus, Systemic, Susceptibility To

  • Lupus Vulgaris

  • Lupus Erythematosus, Discoid

  • Lupus Erythematosus

  • Systemic Lupus Erythematosus Nos

  • Sle - [Systemic Lupus Erythematosus]

Malignant Hyperthermia
  • Anesthesia Related Hyperthermia

  • Malignant Hyperpyrexia Due To Anesthesia

  • Hyperpyrexia, Malignant

  • Hyperthermia, Malignant

  • Malignant Hyperpyrexia

  • Mhs

  • Malignant Fever

Acquired Von Willebrand Syndrome
  • Acquired Von Willebrand Disease

  • Willebrand Disease, Acquired

  • Avws

Granulomatosis With Polyangiitis
  • GPA

  • Wegener Granulomatosis

  • Wegener Granulomatosis, Formerly

  • Midline Granulomatosis

  • Wg, Formerly

  • Necrotizing Respiratory Granulomatosis

  • Wg

  • Wegeners Granulomatosis

  • Pauci-Immune Glomerulonephritis Associated With Granulomatosis With Polyangiitis

Chronic Neutrophilic Leukemia
  • Cnl

  • Leukemia Neutrophilic Chronic

Autoimmune Disease
  • Autoimmune Diseases

  • Autoimmune Hypersensitivity Disease

  • Hypersensitivity Reaction Type Ii Disease

  • Type Ii Hypersensitivity Reaction Disease

Achalasia
  • Cardiospasm

  • Achalasia Of Cardia

  • Esophageal Achalasia

  • Hypertensive Lower Esophageal Sphincter

  • Idiopathic Achalasia

  • Achalasia Cardia

  • Idiopathic Achalasia Of Esophagus

  • Primary Achalasia

  • Achalasia Of Esophagus

  • Lack Of Reflex Relaxation Of Lower Oesophageal Sphincter

  • Aperistalsis Of The Oesophagus

  • Achalasia Of Oesophagus

  • Oesophageal Achalasia

  • Achalasia Nos

  • Cardia Spasm

  • Cardia Achalasia

  • Oesophageal Cardiospasm

  • Oesophagus Achalasia

  • Reflex Cardiospasm

Chronic Eosinophilic Leukemia
  • Pdgfra-Associated Chronic Eosinophilic Leukemia

Congenital Hypothyroidism
  • Cretinism

  • Neonatal Hypothyroidism

  • Ch

  • Cht

  • Congenital Myxedema

  • Myxedema, Congenital

  • Endemic Cretinism

  • Congenital Iodine-Deficiency Syndrome

  • Fetal Iodine Deficiency Syndrome

  • Congenital Iodine-Deficiency Hypothyroidism Nos

Long Qt Syndrome
  • Romano-Ward Syndrome

  • Long Q-T Syndrome

  • Lqt

  • Qt Syndrome, Long

  • Congenital Long Qt Syndrome

  • Familial Long Qt Syndrome

Atypical Chronic Myeloid Leukemia, Bcr-Abl1 Negative
  • Atypical Chronic Myeloid Leukemia

  • Atypical Chronic Myeloid Leukaemia

  • Leukemia, Myeloid, Chronic, Atypical, Bcr-Abl Negative

  • Acml

  • Atypical Chronic Myeloid Leukaemia Bcr-Abl1 Negative

  • Atypical Chronic Myeloid Leukemia Bcr-Abl1 Negative

  • Atypical Cml

  • Subacute Myeloid Leukemia

  • Subacute Myelogenous Leukaemia

  • Subacute Myeloid Leukaemia

  • Subacute Myelosis

  • Atypical Chronic Myeloid Leukaemia, Bcr-Abl-Negative Without Mention Of Remission

  • Subacute Monocytic Leukaemia Without Mention Of Remission

  • Subacute Monocytic Leukaemia

Bone Marrow Cancer
  • Malignant Neoplasm Of Bone Marrow

  • Bone Marrow Neoplasm

  • Bone Marrow Tumor

  • Malignant Bone Marrow Tumor

  • Myeloproliferative Disorders

  • Bone Marrow Neoplasms

  • Myeloproliferative Disease

  • Chronic Myeloproliferative Disorder

Volvulus Of Midgut
  • Volvulus

  • Intestinal Volvulus

  • Intestinal Malrotation, Familial

  • Familial Intestinal Malrotation

  • Twist Of Intestine, Bowel, Or Colon

Lacrimal Gland Mucoepidermoid Carcinoma
  • Mucoepidermoid Carcinoma Of The Lacrimal Gland

Acquired Polycythemia
  • Secondary Polycythemia

  • Polycythemia, Secondary

  • Secondary Erythrocytosis

  • Polycythemia Secondary

Wernicke Encephalopathy
  • Wernicke'S Encephalopathy

  • Wernicke'S Disease

  • Encephalopathy, Wernicke'S

  • Wernicke-Korsakoff Syndrome

  • Encephalopathy Due To Vitamin B1 Deficiency

  • Wernicke Disease

  • Wernicke Syndrome

Pineal Region Meningioma
  • Pineal Meningioma

Cutis Laxa
  • Generalized Elastolysis

  • Loose Skin

  • Dermatolysis

  • Dermatomegaly

  • Cutis Laxa Syndrome

Myeloproliferative Neoplasm
  • Myeloproliferative Disorder

  • Chronic Myeloproliferative Disease

  • Myeloproliferative Neoplasms

  • Chronic Myeloproliferative Disorder

  • Cmpd

  • Cmpd, U

  • Chronic Myeloproliferative Disorders

  • Mpd

  • Mpn

  • Myeloproliferative Disorders

  • Myeloproliferative Disease

  • Campomelic Dysplasia

Dilated Cardiomyopathy
  • Familial Dilated Cardiomyopathy

  • Primary Dilated Cardiomyopathy

  • Idiopathic Dilated Cardiomyopathy

  • Congestive Cardiomyopathy

  • Idiopathic Dilation Cardiomyopathy

  • Primary Familial Dilated Cardiomyopathy

  • Cardiomyopathy, Dilated

  • DCM

  • Cardiomyopathy, Familial Dilated

  • Dilated Cardiomyopathy, Familial

  • Hypokinetic Dilated Cardiomyopathy, Familial

  • Familial Idiopathic Cardiomyopathy

  • Fdc

  • Cardiomyopathy, Familial Idiopathic

  • Idiopathic Cardiomegaly

  • Dilated Congestive Cardiomyopathy

  • Chronic Dilated Cardiomyopathy

  • Ccm - [Congestive Cardiomyopathy]

  • Cocm - [Congestive Cardiomyopathy]

  • Dcm - [Dilated Cardiomyopathy]

  • Dilated-Hypokinetic Cardiomyopathy

  • Congestive Idiopathic Cardiomyopathy

  • Primary Idiopathic Dilated Cardiomyopathy

Celiac Disease 1
  • Celiac Disease

  • Coeliac Disease

  • Celiac Sprue

  • Celiac Disease, Susceptibility To

  • Gluten-Sensitive Enteropathy

  • Nontropical Sprue

  • Sprue

  • CELIAC1

  • Celiac Disease, Susceptibility To, 1

  • Celiac Sprue 1

  • Celiac Sprue, Susceptibility To, 1

  • Gluten-Sensitive Enteropathy 1

  • Gluten-Sensitive Enteropathy, Susceptibility To, 1

  • Idiopathic Steatorrhea

  • Cœliac Disease

  • Gluten Intolerance

  • Gluten-Induced Enteropathy

  • Gluten Enteropathy

  • Celiac Disease, Susceptibility To, Type 1

  • Childhood Celiac Disease

  • Coeliac Rickets

  • Gee Disease

  • Gee-Herter Disease

  • Heubner-Herter Disease

  • Idiopathic Steatorrhoea

  • Thaysen'S Disease

  • Herter Gee Syndrome

Thrombocytopenia
  • Low Platelet Count

  • Low Platelets

  • Decreased Platelets

  • Platelet Dysfunction Nos

Myelodysplastic/Myeloproliferative Neoplasm
  • Myelodysplastic-Myeloproliferative Diseases

  • Myelodysplastic/Myeloproliferative Disease

  • Myelodysplastic Myeloproliferative Cancer

  • Myelodysplastic Myeloproliferative Disease

  • Myeloproliferative/Myelodysplastic Syndromes

Bladder Cancer
  • Urinary Bladder Cancer

  • Bladder Carcinoma

  • Urinary Bladder Carcinoma

  • Bladder Neoplasm

  • Bladder Tumor

  • Cancer, Bladder

  • Malignant Neoplasm Of Urinary Bladder

  • Carcinoma Of Bladder

  • Bladder Cancer, Somatic

  • Tumor Of The Bladder

  • Carcinoma Of Urinary Bladder

  • Bladder Carcinoma Urinary

  • Cancer Of The Urinary Bladder

  • Cancer, Urinary Bladder

  • Malignant Bladder Neoplasm

  • Malignant Bladder Tumor

  • Neoplasm Of The Bladder

  • Neoplasm Of The Urinary Bladder

  • Tumor Of The Urinary Bladder

  • Urinary Bladder Neoplasm

  • BLC

  • Urothelial Carcinoma Of The Bladder

  • Bladder Tumors

  • Urinary Bladder Neoplasms

  • Bladder Cancer Nos

  • Vesical Cancer Nos

  • Malignant Neoplasm Of Bladder, Part Unspecified

  • Malignant Tumour Of Urinary Bladder

  • Primary Malignant Neoplasm Of Bladder

Colorectal Cancer
  • Colon Cancer

  • Colorectal Carcinoma

  • Colon Carcinoma

  • Colorectal Cancer, Susceptibility To

  • Carcinoma Of Colon

  • CRC

  • Colorectal Cancer With Chromosomal Instability, Somatic

  • Colon Cancer, Somatic

  • Colon Cancer, Susceptibility To

  • Colonic Neoplasms

  • Colorectal Neoplasms

  • Colorectal Cancer, Somatic

  • Colon Cancer, Advanced, Somatic

  • Colonic Carcinoma

  • Colorectal Carcinomas

  • Colon Cancers

  • Colorectal Cancers

  • Cancer, Colorectal, Somatic

  • Cancer, Colon

  • Cancer, Colorectal, Susceptibility To

  • Colorectal Neoplasm

  • Colonic Neoplasm

  • Malignant Tumor Of Colon

Hypertrophic Cardiomyopathy
  • Hypertrophic Obstructive Cardiomyopathy

  • Cardiomyopathy, Hypertrophic

  • Cardiomyopathy Hypertrophic Obstructive

  • Cardiomyopathy, Hypertrophic, Familial

  • Idiopathic Myocardial Hypertrophy

  • Idiopathic Hypertrophic Cardiomyopathy

  • Obstructive Idiopathic Hypertrophic Cardiomyopathy

  • Obstructive Cardiomyopathy

  • Idiopathic Hypertrophic Subaortic Stenosis

  • Muscular Subaortic Stenosis

  • Hypertrophic Obstructive Subaortic Stenosis

Erythromelalgia
  • Primary Erythromelalgia

  • Erythermalgia

  • Primary Erythermalgia

  • Mitchell Disease

  • Familial Erythromelalgia

Developmental And Epileptic Encephalopathy 60
  • DEE60

  • Epileptic Encephalopathy, Early Infantile, 60

  • Eiee60

  • Developmental And Epileptic Encephalopathy, 60

  • Early Infantile Epileptic Encephalopathy 60

Blood Platelet Disease
  • Platelet Disorder

  • Blood Platelet Disorders

  • Thrombocytopathy

  • Platelet Dysfunction

  • Platelet Disorders

  • Qualitative Platelet Deficiency

Prostate Cancer
  • Prostate Carcinoma

  • Prostate Cancer, Familial

  • Prostate Neoplasm

  • Prostate Cancer, Somatic

  • Prostate Cancer, Susceptibility To

  • Prostatic Cancer

  • Prostatic Neoplasms

  • Hereditary Prostate Cancer

  • Prostatic Neoplasm

  • Cancer Of Prostate

  • Carcinoma Of Prostate

  • Familial Prostate Cancer

  • Familial Prostate Carcinoma

  • Malignant Tumor Of Prostate

  • Malignant Neoplasm Of Prostate

  • Prostate Cancer, Familial, Susceptibility To

  • Malignant Tumor Of The Prostate

  • Ngp - New Growth Of Prostate

  • Tumor Of The Prostate

  • Prostate Cancer, Hereditary

  • Cancer Of The Prostate

  • Malignant Neoplasm Of The Prostate

  • Prostatic Carcinoma

  • PC

  • Prca

  • Cancer, Prostate

  • Malignant Prostatic Tumour

  • Malignant Tumour Of Prostate

  • Primary Prostate Cancer

  • Primary Malignant Neoplasm Of Prostate

  • Prostate Gland Cancer

Hemochromatosis, Type 1
  • Hemochromatosis

  • Hemochromatosis Type 1

  • Hereditary Hemochromatosis

  • Hh

  • HFE1

  • Hfe Hemochromatosis, Modifier Of

  • Symptomatic Form Of Classic Hemochromatosis

  • Symptomatic Form Of Hemochromatosis Type 1

  • Symptomatic Form Of Hfe-Related Hereditary Hemochromatosis

  • Haemochromatosis

  • Iron Storage Disorder

  • Bronze Diabetes

  • Hereditary Haemochromatosis

  • Hlah

  • Hfe

  • Hemochromatosis, Hereditary

  • Diabetes Bronze

  • Classic Hemochromatosis

  • Hfe-Associated Hereditary Hemochromatosis

  • Hemochromatosis Classic

  • Bronzed Cirrhosis

  • Familial Hemochromatosis

  • Genetic Hemochromatosis

  • Hc

  • Pigmentary Cirrhosis

  • Primary Hemochromatosis

  • Troisier-Hanot-Chauffard Syndrome

  • Von Recklenhausen-Applebaum Disease

  • Hemochromatosis 1

  • Primary Hereditary Hemochromatosis

  • Bronze Cirrhosis

Blood Coagulation Disease
  • Blood Coagulation Disorders

  • Coagulation Protein Disease

  • Inherited Blood Coagulation Disease

  • Postpartum Coagulation Defect

  • Postpartum Coagulation Defect With Delivery

  • Coagulation Protein Disorders

  • Puerperal Coagulopathy

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

Chronic Myelomonocytic Leukemia
  • Leukemia, Myelomonocytic, Chronic

  • Cmml

  • Leukemia Myelomonocytic Chronic

  • Cmml - [Chronic Myelomonocytic Leukaemia]

  • Chronic Myelomonocytic Leukaemia Without Mention Of Remission

  • Chronic Monocytic Leukaemia

  • Chronic Monocytoid Leukaemia

Cystic Fibrosis
  • Mucoviscidosis

  • CF

  • Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis

  • Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis

  • Cystic Fibrosis Lung Disease, Modifier Of

  • Cystic Fibrosis Of Pancreas

  • Fibrocystic Disease Of Pancreas

  • Cf - [Cystic Fibrosis]

  • Cystic Fibrosis Nos

  • Fibrocystic Disease

  • Fibrocystic Disease Of The Pancreas

  • Mucoviscidosis Of Pancreas

  • Nonproliferative Fibrocystic Disease

  • Pancreatic Cystic Fibrosis

Diffuse Large B-Cell Lymphoma Activated B-Cell Type
  • Dlbcl Abc Type

Mixed Oligodendroglioma-Astrocytoma
  • Who Grade Ii Mixed Glioma

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

Connective Tissue Disease
  • Connective Tissue Diseases

  • Connective Tissue Disorder

  • Abnormality Of Connective Tissue

  • Disorder Of Connective Tissue

  • Connective Tissue Disorders

Developmental And Epileptic Encephalopathy 11
  • Epileptic Encephalopathy, Early Infantile, 11

  • DEE11

  • Eiee11

  • Developmental And Epileptic Encephalopathy, 11

  • Early Infantile Epileptic Encephalopathy 11

  • Encephalopathy, Developmental And Epileptic, Type 11

Primary Biliary Cholangitis
  • Primary Biliary Cirrhosis

  • Biliary Liver Cirrhosis

  • Chronic Nonsuppurative Destructive Cholangitis

  • Familial Primary Biliary Cirrhosis

  • Pbc

  • Hanot Syndrome

  • Cholestatic Cirrhosis

  • Biliary Cirrhosis Primary

  • Liver Cirrhosis, Biliary

  • Hanot'S Cirrhosis

  • Biliary Cirrhosis

  • Pericholangiolic Biliary Cirrhosis

  • Tannhauser-Magendantz Syndrome

  • Hanot-Rossle Syndrome

  • Hypertrophic Cirrhosis

  • Todd Cirrhosis

  • Hanot Cirrhosis

  • Charcot Cirrhosis

  • Mahon-Tannhauser Syndrome

  • Toxic Cirrhosis

  • Hypertrophic Biliary Cirrhosis

  • Monolobular Cirrhosis

  • Unilobar Cirrhosis

  • Xanthomatous Biliary Cirrhosis

Myelodysplastic Syndrome
  • Myelodysplastic Syndromes

  • Myelodysplasia

  • MDS

  • Myelodysplastic Syndrome Included

  • Myelodysplastic Syndrome, Susceptibility To, Included

  • Myelodysplastic Syndrome, Somatic

  • Myelodysplastic Syndrome, Susceptibility To

Leukemia, Acute Myeloid
  • Acute Myeloid Leukemia

  • Leukemia, Acute Myelogenous

  • Acute Myelogenous Leukemia

  • AML

  • Leukemia, Acute Myeloid, Susceptibility To

  • Acute Myeloblastic Leukemia

  • Leukemia, Acute Myeloid, Reduced Survival In, Somatic

  • Acute Myeloid Leukaemia

  • Leukemia, Myelocytic, Acute

  • Therapy Related Acute Myeloid Leukemia And Myelodysplastic Syndrome

  • Secondary Aml

  • Acute Myelocytic Leukemia

  • Acute Myeloid Leukemia, Somatic

  • Leukemia, Acute Myeloid, Somatic

  • Myeloid Leukemia, Acute, M4/M4eo Subtype, Somatic

  • Acute Myeloblastic Leukaemia

  • Acute Myelogenous Leukaemia

  • Aml - Acute Myeloid Leukemia

  • Acute Myeloid Leukemia With Cebpa Somatic Mutations

  • Aml With Cebpa Somatic Mutations

  • Inherited Acute Myeloid Leukemia

  • Familial Aml

  • Inherited Aml

  • Pure Familial Aml

  • Pure Familial Acute Myeloid Leukemia

  • Secondary Acute Myeloid Leukemia

  • Therapy-Related Aml And Myelodysplastic Syndrome

  • Acute Myeloid Leukemia, Secondary

  • Acute Non-Lymphoblastic Leukemia

  • Acute Non-Lymphocytic Leukemia

  • Acute Biphenotypic Leukemia

  • Acute Undifferentiated Leukemia

  • Acute Myeloblastic Leukaemia With Multilineage Dysplasia

  • Acute Myeloid Leukaemia With Multilineage Dysplasia Without Mention Of Remission

  • Acute Myeloid Leukaemia With Myelodysplasia-Related Features

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

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
Rattus norvegicus CALR RGD RGD:620288
Canis familiaris CALR VGNC VGNC:54585
Bos taurus CALR VGNC VGNC:26715
Felis catus CALR VGNC VGNC:60327
Mus musculus CALR MGD MGI:88252
Macaca mulatta CALR VGNC VGNC:70519
Others CALR NCBI