| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An autosomal dominant disease characterized by abnormal development of ectodermal tissues including the skin, hair, nails, teeth and sweat glands and anhidrotic ectodermal dysplasia with cleft lip/palate. (Human Disease Ontology, DOID_0060330) |
| External Link | http://www.omim.org/entry/129400 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the rapp-hodgkin syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| TP63 | tumor protein p63 |
