Female Pseudohermaphroditism Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	Hermaphroditism refers to a discrepancy between the morphology of the gonads and that of the external genitalia. In female pseudohermaphroditism, the genotype is female (XX) and the gonads are ovaries, but the external genitalia are virilized. (Human Phenotype Ontology, HP_0010458)
External Link	https://www.disgenet.org/browser/0/1/0/C0238394
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Genes

10 genes associated with the disease Female Pseudohermaphroditism in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
AR	androgen receptor
CD96	CD96 molecule
CYP19A1	cytochrome P450, family 19, subfamily A, polypeptide 1
CYP2B6	cytochrome P450, family 2, subfamily B, polypeptide 6
FRAS1	Fraser extracellular matrix complex subunit 1
FREM2	FRAS1 related extracellular matrix protein 2
GRIP1	glutamate receptor interacting protein 1
INSR	insulin receptor
NR3C1	nuclear receptor subfamily 3, group C, member 1 (glucocorticoid receptor)
SPECC1L	sperm antigen with calponin homology and coiled-coil domains 1-like