DISEASES

Disease-gene associations mined from literature

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Human genes for erythrokeratodermia variabilis

Erythrokeratodermia variabilis [DOID:0050467]

A skin disease that is characterized by areas of sharply demarcated, brown hyperkeratosis and has_material_basis_in mutations in genes encoding for connexin channels proteins in the epidermis.

Synonyms:  erythrokeratodermia variabilis,  DOID:0050467,  erythrokeratodermia variabilises,  Erythrokeratodermia Figurata Variabilis,  Greither Disease ...

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.