Osteochondrodysplasias

Osteochondrodysplasias

Osteochondrodysplasia
Classification and external resources

ICD-10 Q 77.-Q 78.

MeSH D010009

Osteochondrodysplasia is a general term for a disorder of the development (dysplasia) of bone ("osteo") and cartilage ("chondro").^[1]

Types

Examples include:

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v • d • e Osteochondrodysplasia (Q77-Q78, 756.4-756.5)

Osteodysplasia/ osteodystrophy	Osteosclerosis (Raine syndrome) - Osteopoikilosis - Osteopetrosis - Boomerang dysplasia - Hereditary multiple exostoses - Otospondylomegaepiphyseal dysplasia - Fibrous dysplasia (McCune-Albright syndrome)

Chondrodysplasia/ chondrodystrophy	Achondrogenesis/Hypochondrogenesis - Chondrodysplasia punctata (Rhizomelic chondrodysplasia punctata, Conradi-Hünermann syndrome) - Achondroplasia (Hypochondroplasia)

Both/ungrouped	Thanatophoric dysplasia - Short rib-polydactyly syndrome - Ellis-van Creveld syndrome - Spondyloepiphyseal dysplasia congenita - Metaphyseal dysplasia - Multiple epiphyseal dysplasia (Recessive) - Atelosteogenesis, type II - Diastrophic dysplasia - Camurati-Engelmann disease - Antley-Bixler syndrome - Skeletal dysplasia

Collagen diseases	Osteogenesis imperfecta - Ehlers-Danlos syndrome

See also osteochondropathy, neoplasia