DISEASES

Disease-gene associations mined from literature

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Human genes for persistent hyperplastic primary vitreous

Persistent hyperplastic primary vitreous [DOID:0060282]

A developmental vitreous disease that is characterized by leukocoria, strabismus and vision loss, caused by failure of primary vitreous and hyaloid vasculature to regress during embryological development.

Synonyms:  persistent hyperplastic primary vitreous,  DOID:0060282,  persistent hyperplastic primary vitreouses,  persistent hyperplastic primary vitreoi

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.