DISEASES

Disease-gene associations mined from literature

SearchDownloadsAbout

Human genes for hemochromatosis type 2B

Hemochromatosis type 2B [DOID:0111032]

A hemochromatosis type 2 that has_material_basis_in homozygous mutation in the HAMP gene on chromosome 19q13.

Synonyms:  hemochromatosis type 2B,  DOID:0111032,  HFE2B

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.