DISEASES

Disease-gene associations mined from literature

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Human genes for persistent Mullerian duct syndrome

Persistent Mullerian duct syndrome [DOID:0050791]

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.

Synonyms:  persistent Mullerian duct syndrome,  DOID:0050791,  persistent Mullerian duct disease,  persistent Mullerian duct disorder,  persistent Mullerian duct syndromes ...

Linkouts:  OMIM

The disease-gene associations are derived from automatic text mining of the biomedical literature, manually curated database annotations, cancer mutation data, and genome-wide association studies. The confidence of each association is signified by stars, where ★★★★★ is the highest confidence and ★☆☆☆☆ is the lowest.

Developed by Sune Frankild, Alexander Junge, Albert Pallejà, Dhouha Grissa, Kalliopi Tsafou, and Lars Juhl Jensen from the Novo Nordisk Foundation Center for Protein Research.