cerebral hemorrhage Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Hemorrhage into the parenchyma of the brain. (Human Phenotype Ontology, HP_0001342)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001342
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Genes

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

Symbol Name
ABCC6 ATP-binding cassette, sub-family C (CFTR/MRP), member 6
ACVRL1 activin A receptor type II-like 1
APP amyloid beta (A4) precursor protein
CPT2 carnitine palmitoyltransferase 2
ENG endoglin
JAK2 Janus kinase 2
KIF1B kinesin family member 1B
PDCD10 programmed cell death 10
RET ret proto-oncogene
SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
SDHD succinate dehydrogenase complex, subunit D, integral membrane protein
SH2B3 SH2B adaptor protein 3
VHL von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase