DISEASES

Disease-gene associations mined from literature

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Human genes for 46 XX gonadal dysgenesis

46 XX gonadal dysgenesis [DOID:14450]

A gonadal dysgenesis that is characterized by the lack of functional ovaries to induce puberty in an otherwise 46,XX female.

Synonyms:  46 XX gonadal dysgenesis,  DOID:14450,  ovarian dysgenesis,  ovarian dysgenesises

Linkouts:  OMIM #1 #2 #3

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.