cerebral hamartomata Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description The presence of a hamartoma of the cerebrum. (Human Phenotype Ontology, HP_0009731)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0009731
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5 genes associated with the cerebral hamartomata phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
GLI3 GLI family zinc finger 3
OFD1 oral-facial-digital syndrome 1
SOX2 SRY (sex determining region Y)-box 2
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2