DISEASES

Disease-gene associations mined from literature

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Human genes for autosomal dominant dyskeratosis congenita 3

Autosomal dominant dyskeratosis congenita 3 [DOID:0070018]

A dyskeratosis congenita that has_material_basis_in an autosomal dominant mutation of TINF2 on chromosome 14q12.

Synonyms:  autosomal dominant dyskeratosis congenita 3,  DOID:0070018,  DKCA3

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.