Persistent Mullerian duct syndrome Gene Set

Dataset CTD 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 http://ctdbase.org/detail.go?type=disease&acc=MESH:C536665
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Genes

2 genes/proteins associated with the disease Persistent Mullerian duct syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
AMH anti-Mullerian hormone 2.88009
AMHR2 anti-Mullerian hormone receptor, type II 2.88009