adrenal insufficiency, congenital, with 46xy sex reversal, partial or complete Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_0050546)
External Link http://www.omim.org/entry/613743
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Genes

1 genes associated with the adrenal insufficiency, congenital, with 46xy sex reversal, partial or complete phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
CYP11A1 cytochrome P450, family 11, subfamily A, polypeptide 1