|Dataset||OMIM Gene-Disease Associations|
|Category||disease or phenotype associations|
|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)|
|Downloads & Tools|
1 genes associated with the smith-mccort dysplasia phenotype from the curated OMIM Gene-Disease Associations dataset.