ambiguous genitalia, male Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Ambiguous genitalia in an individual with XY genetic gender. (Human Phenotype Ontology, HP_0000033)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000033
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Genes

7 genes associated with the ambiguous genitalia, male phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DHCR24 24-dehydrocholesterol reductase
MKS1 Meckel syndrome, type 1
SC5D sterol-C5-desaturase
SRD5A2 steroid-5-alpha-reductase, alpha polypeptide 2 (3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 2)
TBX15 T-box 15
TSPYL1 TSPY-like 1
WT1 Wilms tumor 1