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Disease Ontology Browser
Smith-McCort dysplasia (DOID:0060247)
Alt IDs: OMIM:607326, OMIM:615222, MESH:C564589, ORDO:178355, UMLS_CUI:C1846431
Definition: An osteochondrodysplasia characterized by short limbs and a short trunk with a barrel-shaped chest and has material basis in homozygous or compound heterozygous mutation in the DYM gene on chromosome 18q.

Disease References using Mouse Models (1)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
06/13/2017
MGI 6.10
The Jackson Laboratory