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
Similar Terms
Downloads & Tools


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