Bruck syndrome 2

MONDO:0012217

Any Bruck syndrome in which the cause of the disease is a mutation in the PLOD2 gene.

Also known as: Bruck syndrome 2, Bruck syndrome caused by mutation in PLOD2, Bruck syndrome type 2, PLOD2 Bruck syndrome, BRKS2, osteogenesis imperfecta with congenital Joint contractures

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) Syndromic disease (25) Human disease (14) Osteochondrodysplasia (12) Skeletal system disorder (4) Bone development disease (2)

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