DISEASES

Disease-gene associations mined from literature

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Human genes for hereditary lymphedema II

Hereditary lymphedema II [DOID:0070213]

A hereditary lymphedema characterized by onset around puberty of chronic lymphedema particularly in the lower limbs with an apparent autosomal dominant pattern of inheritance.

Synonyms:  hereditary lymphedema II,  DOID:0070213,  familial lymphedema II,  hereditary lymphedema IIs,  late-onset 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.