DISEASES

Disease-gene associations mined from literature

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Human genes for ectodermal dysplasia 5

Ectodermal dysplasia 5 [DOID:0111657]

A pure hair and nail ectodermal dysplasia that has_material_basis_in homozygous or compound heterozygous mutation in a region on chromosome 10q24.32-q25.1.

Synonyms:  ectodermal dysplasia 5,  DOID:0111657,  ECTD5,  ectodermal dysplasia 5, hair/nail type,  ectodermal dysplasia 5 hair/nail type ...

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.