Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Echinobase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Echinobase
Summary Literature (0)
DOID:0060247 - Smith-McCort dysplasia

Disease Ontology Definition:A Syggve-Melchior-Clausen disease 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.

Synonyms:

Echinobase Genes :


OMIM:
MIM:607326 - smith-mccort dysplasia 1; smc1
MIM:615222 - smith-mccort dysplasia 2; smc2

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): Dyggve-Melchior-Clausen disease (is_a)