autoimmune hemolytic anemia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An autoimmune disease of blood that is characterized by deficient red blood cells caused by auto-antibodies. (Human Disease Ontology, DOID_718)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001890
Similar Terms
Downloads & Tools

Genes

10 genes associated with the autoimmune hemolytic anemia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ADA adenosine deaminase
CASP10 caspase 10, apoptosis-related cysteine peptidase
CD3G CD3g molecule, gamma (CD3-TCR complex)
FAS Fas cell surface death receptor
FASLG Fas ligand (TNF superfamily, member 6)
FOXP3 forkhead box P3
LRBA LPS-responsive vesicle trafficking, beach and anchor containing
NBN nibrin
PNP purine nucleoside phosphorylase
STIM1 stromal interaction molecule 1