DISEASES

Disease-gene associations mined from literature

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Human genes for familial hemophagocytic lymphohistiocytosis 3

Familial hemophagocytic lymphohistiocytosis 3 [DOID:0110923]

A hemophagocytic lymphohistiocytosis that has_material_basis_in a mutation of UNC13D on chromosome 17q25.1.

Synonyms:  familial hemophagocytic lymphohistiocytosis 3,  DOID:0110923,  hereditary hemophagocytic lymphohistiocytosis 3,  HLH3,  HPLH3

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.