Smith-McCort dysplasia https://rarediseases.info.nih.gov/diseases/10620/smith-mccort-dysplasia https://www.malacards.org/card/smith_mccort_dysplasia Orphanet:178355 SCTID:715862006 Smith-McCort dwarfism UMLS:C1846431 MONDO:0015799 Smith-McCort dysplasia (SMC) is a rare spondylo-epi-metaphyseal dysplasia characterized by the clinical manifestations of coarse facies, short neck, short trunk dwarfism with barrel-shaped chest and rhizomelic limb shortening, as well as specific radiological features (i.e. generalized platyspondyly with double-humped vertebral end plates and iliac crests with a lace-like appearance) and normal intelligence. The clinical and skeletal features are similar to those seen in the allelic disorder Dyggve-Melchior-Clausen syndrome (DMC), but can be distinguished from this syndrome by the absence of intellectual deficiency and microcephaly in SMC. MEDGEN:375887 MESH:C564589 icd11.foundation:1800275830 OMIMPS:607326 Smith McCort dysplasia GARD:0010620 DOID:0060247 spondyloepiphyseal dysplasia