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Leri-Weill dyschondrosteosis

Disease Summary
Associated Targets (1)
Tbio

1


GARD Rare
Mondo Description LC)ri-Weill dyschondrosteosis (LWD) is a skeletal dysplasia marked by disproportionate short stature and the characteristic Madelung wrist deformity.
Uniprot Description Dominantly inherited skeletal dysplasia characterized by moderate short stature predominantly because of short mesomelic limb segments. It is often associated with the Madelung deformity of the wrist, comprising bowing of the radius and dorsal dislocation of the distal ulna.
Disease Ontology Description An osteochondrodysplasia characterized by abnormal shortening of the forearms and lower legs, abnormal misalignment of the wrist (Madelung deformity of the wrist), and associated short stature and has_material_basis_in heterozygous defects in the pseudoautosomal genes SHOX or SHOXY or by deletion of the SHOX downstream regulatory domain.
Mondo Term and Equivalent IDs
MONDO:0007481:  Leri-Weill dyschondrosteosis
GARD:0003224: 
NCIT:C126560: 
Orphanet:240: 
SCTID:17818006: 
UMLS:C0265309: