| Dataset | CTD Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | disease |
| Description | Acrofacial dysostosis, Weyers type (WAD) is a rare ectodermal dysplasia syndrome with bone abnormalities, characterized by postaxial polydactyly, onychodystrophy, dental anomalies, and a mild short stature associated with normal intelligence. (Orphanet Rare Disease Ontology, Orphanet_952) |
| External Link | http://ctdbase.org/detail.go?type=disease&acc=MESH:C536695 |
| Similar Terms | |
| Downloads & Tools |
1 genes/proteins associated with the disease Weyers acrofacial dysostosis from the curated CTD Gene-Disease Associations dataset.
| Symbol | Name | Standardized Value |
|---|---|---|
| EVC | Ellis van Creveld protein | 2.88009 |
