DISEASES

Disease-gene associations mined from literature

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Human genes for congenital generalized lipodystrophy

Congenital generalized lipodystrophy [DOID:0050585]

A lipodystrophy that is characterized by extreme scarcity of subcutaneous fat, muscular hypertrophy, fatty liver, hypertriglyceremia and metabolic complications including insulin resistance.

Synonyms:  congenital generalized lipodystrophy,  congenital generalized lipodystrophies,  DOID:0050585

Linkouts:  OMIM #1 #2 #3 #4

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.