ambiguous genitalia, female Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Ambiguous genitalia in an individual with XX genetic gender. (Human Phenotype Ontology, HP_0000061)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000061
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Genes

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

Symbol Name
CYP11B1 cytochrome P450, family 11, subfamily B, polypeptide 1
DHCR24 24-dehydrocholesterol reductase
MKS1 Meckel syndrome, type 1
TBX15 T-box 15
TNXB tenascin XB
WT1 Wilms tumor 1