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Disease Ontology Browser
spondylometaepiphyseal dysplasia, short limb-hand type (DOID:0112196)
Alliance: disease page
Synonyms: SMED short limb-abnormal calcification type; SMED short limb-hand type; SMED type 2; SMED, type II; SMED-SL; SMED-SL/AC; spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome; spondylometaepiphyseal dysplasia short limb-hand type
Alt IDs: OMIM:271665, MESH:C564794, ORDO:93358, UMLS_CUI:C1849011
Definition: A spondyloepimetaphyseal dysplasia characterized by short stature, short limbs and hands, and typical radiological features which include platyspondyly, metaphyseal, and epiphyseal involvement, short tubular bones of the limbs, and abnormal calcification of cartilage that has_material_basis_in homozygous or compound heterozygous mutation in the DDR2 gene on chromosome 1q23.3.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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12/10/2024
MGI 6.24 		The Jackson Laboratory