DISEASES

Disease-gene associations mined from literature

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Human genes for Gamstorp-Wohlfart syndrome

Gamstorp-Wohlfart syndrome [DOID:0050526]

A syndrome characterized by progressive weakness and atrophy of muscles in feet, legs and hands. In some patients the syndrome also causes decreased sensitivity to touch, heat or cold, particularly in the lower arms or legs.

Synonyms:  Gamstorp-Wohlfart syndrome,  DOID:0050526,  GamstorpWohlfart syndrome,  Gamstorp-Wohlfart disease,  Gamstorp-Wohlfart disorder ...

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.