cerebellar hemorrhage Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Hemorrhage into the parenchyma of the cerebellum. (Human Phenotype Ontology, HP_0011695)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0011695
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Genes

5 genes associated with the cerebellar hemorrhage phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
APP amyloid beta (A4) precursor protein
IVD isovaleryl-CoA dehydrogenase
MUT methylmalonyl CoA mutase
PCCA propionyl CoA carboxylase, alpha polypeptide
PCCB propionyl CoA carboxylase, beta polypeptide