DISEASES

Disease-gene associations mined from literature

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Human genes for dermatopathia pigmentosa reticularis

Dermatopathia pigmentosa reticularis [DOID:0111342]

An ectodermal dysplasia characterized by reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy that has_material_basis_in heterozygous mutation in KRT14 on chromosome 17q21.2.

Synonyms:  dermatopathia pigmentosa reticularis,  dermatopathia pigmentosa reticularises,  DOID:0111342,  DPR

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.