DISEASES

Disease-gene associations mined from literature

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Human genes for hereditary lymphedema I

Hereditary lymphedema I [DOID:0070212]

A hereditary lymphedema characterized by autosomal dominant inheritance of chronic, generally painless, lower limb lymphedema with onset typically at birth or in early childhood.

Synonyms:  hereditary lymphedema I,  DOID:0070212,  familial lymphedema I,  hereditary lymphedema Is,  congenital primary lymphedema ...

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.