DISEASES

Disease-gene associations mined from literature

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Human genes for reticulate acropigmentation of Kitamura

Reticulate acropigmentation of Kitamura [DOID:0060258]

A pigmentation disease characterized by lesions that initially arise as letiginous, hyperpigmented macules in a reticular pattern on the dorsal aspect of the hands and feet. Over time, lesions may spread proximally and may darken; palmoplantar pitting and dermatoglyphic disruption may also be present.

Synonyms:  reticulate acropigmentation of Kitamura,  DOID:0060258,  reticulate acropigmentation of Kitamuras,  RAPK

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.