osteochondrodysplasia omodysplasia https://github.com/monarch-initiative/mondo/issues/6751 https://github.com/monarch-initiative/mondo/issues/6877 https://www.malacards.org/card/omodysplasia GARD:0016608 Omodysplasia is a rare skeletal dysplasia characterized by severe limb shortening and facial dysmorphism. Two types of omodysplasia have been described: an autosomal recessive or generalized form (also referred to as micromelic dysplasia with dislocation of radius) marked by severe micromelic dwarfism with predominantly rhizomelic shortening of both the upper and lower limbs, and an autosomal dominant form in which stature is normal and shortening is limited to the upper limbs. OMIMPS:258315 DOID:0060288 MEDGEN:1388973 SCTID:725164008 UMLS:C4510897 MONDO:0017136 icd11.foundation:1081897527 Orphanet:2733 skeletal dysplasia