Persistent Mullerian Duct Syndrome Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A pseudohermaphroditism that is characterized by the persistence of Mullerian duct derivatives (i.e. uterus, cervix, fallopian tubes and upper two thirds of vagina) in a phenotypically and karyotypically male. (Human Disease Ontology, DOID_0050791)
External Link	https://www.disgenet.org/browser/0/1/0/C1849930
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Genes

8 genes associated with the disease Persistent Mullerian Duct Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
AMH	anti-Mullerian hormone
AMHR2	anti-Mullerian hormone receptor, type II
CLK1	CDC-like kinase 1
CLK2	CDC-like kinase 2
IGF1	insulin-like growth factor 1 (somatomedin C)
NR5A1	nuclear receptor subfamily 5, group A, member 1
QRSL1	glutaminyl-tRNA synthase (glutamine-hydrolyzing)-like 1
SHANK3	SH3 and multiple ankyrin repeat domains 3