| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An autosomal dominant disease that is characterized by fusion of the carpals, tarsals, and phalanges, short first metacarpals causing brachydactyly; and humeroradial fusion. (Human Disease Ontology, DOID_0050789) |
| External Link | http://www.omim.org/entry/186570 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the tarsal-carpal coalition syndrome phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| NOG | noggin |
