|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
2 genes/proteins associated with the disease Persistent Mullerian duct syndrome from the curated CTD Gene-Disease Associations dataset.