recurrent cerebral hemorrhage Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Recurrent bleeding into the parenchyma of the brain. (Human Phenotype Ontology, HP_0004968)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004968
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Genes

1 genes associated with the recurrent cerebral 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