DISEASES

Disease-gene associations mined from literature

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Human genes for Rapp-Hodgkin syndrome

Rapp-Hodgkin syndrome [DOID:0060330]

An ectodermal dysplasia characterized by abnormal development of ectodermal tissues including the skin, hair, nails, teeth and sweat glands and anhidrotic ectodermal dysplasia with cleft lip/palate.

Synonyms:  Rapp-Hodgkin syndrome,  DOID:0060330,  RappHodgkin syndrome,  Rapp-Hodgkin disease,  Rapp-Hodgkin disorder ...

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.