| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| Description | An osteochondrodysplasia characterized by short limbs and a short trunk with a barrel-shaped chest and caused_by homozygous or compound heterozygous mutation in the DYM gene on chromosome 18q. (Human Disease Ontology, DOID_0060247) |
| External Link | http://www.omim.org/entry/607326 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the smith-mccort dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| DYM | dymeclin |
