DISEASES

Disease-gene associations mined from literature

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Human genes for hereditary lymphedema IA

Hereditary lymphedema IA [DOID:0070210]

A hereditary lymphedema characterized by autosomal dominant inheritance that has_material_basis_in mutation in the FLT4 gene on chromosome 5q35.

Synonyms:  hereditary lymphedema IA,  DOID:0070210,  familial lymphedema IA,  hereditary lymphedema IAs,  LMPH1A

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.