| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| 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://www.omim.org/entry/193530 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the weyers acrodental dysostosis phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| EVC | Ellis van Creveld protein |
