| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| 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://ctdbase.org/detail.go?type=disease&acc=MESH:C535289 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Rapp-Hodgkin syndrome from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| TP63 | tumor protein p63 | 2.88009 |
