DISEASES

Disease-gene associations mined from literature

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Human genes for posterior polymorphous corneal dystrophy

Posterior polymorphous corneal dystrophy [DOID:0060457]

A corneal dystrophy that is characterised by changes in Descemet's membrane and endothelial layer.

Synonyms:  posterior polymorphous corneal dystrophy,  DOID:0060457,  posterior polymorphous corneal dystrophies,  hereditary polymorphus posterior corneal dystrophy,  PPCD ...

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.