Craniodiaphyseal dysplasia, autosomal dominant

MONDO:0021021

Also known as: CDD, craniodiaphyseal dysplasia, autosomal dominant, Schaefer Stein Oshman syndrome, craniodiaphyseal dysplasia, dominant, dominantly inherited craniodiaphyseal dysplasia

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Broader categories

Disease (680) Musculoskeletal system disorder (207) Hereditary disease (176) Bone disorder (51) Human disease (14) Bone remodeling disease (5) Skeletal system disorder (4) Disease of genetic or genomic mechanism (2) Craniometaphyseal dysplasia (1) Osteosclerosis (1)

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