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COL1A2-related osteogenesis imperfecta

MONDO:0100596

Any osteogenesis imperfecta in which the cause of the disease is a variant in the COL1A2 gene.

0 clinical trials for this condition and its sub-types.

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Broader categories

Disease (680) Musculoskeletal system disorder (207) Hereditary disease (176) Bone disorder (51) Osteogenesis imperfecta (34) Human disease (14) Osteochondrodysplasia (12) Skeletal system disorder (4) Bone development disease (2) Disease of genetic or genomic mechanism (2)

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