cerebral hypoplasia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Underdevelopment of the cerebrum. (Human Phenotype Ontology, HP_0006872)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0006872
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Genes

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

Symbol Name
BRAF B-Raf proto-oncogene, serine/threonine kinase
BUB1B BUB1 mitotic checkpoint serine/threonine kinase B
DHCR7 7-dehydrocholesterol reductase
FH fumarate hydratase
HSD17B4 hydroxysteroid (17-beta) dehydrogenase 4
MKS1 Meckel syndrome, type 1
RNU4ATAC RNA, U4atac small nuclear (U12-dependent splicing)