DISEASES

Disease-gene associations mined from literature

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Human genes for familial partial lipodystrophy type 1

Familial partial lipodystrophy type 1 [DOID:0070207]

A familial partial lipodystrophy characterized by loss of adipose tissue that is confined to the extremities with normal or increased fat in other areas of the body.

Synonyms:  familial partial lipodystrophy type 1,  DOID:0070207,  hereditary partial lipodystrophy type 1,  familial partial lipodystrophy Kobberling type,  FPLD1 ...

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.