Osteogenesis imperfecta type 14

MONDO:0014029

Any osteogenesis imperfecta in which the cause of the disease is a mutation in the TMEM38B gene.

Also known as: OI14, TMEM38B osteogenesis imperfecta, osteogenesis imperfecta caused by mutation in TMEM38B, OI, type 14, osteogenesis imperfecta, type 14, osteogenesis imperfecta, type XIV

0 clinical trials for this condition and its sub-types, 0 tagged with Osteogenesis imperfecta type 14 itself.

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Part of

↑ Osteogenesis imperfecta and a reduction of bone mineral density. (307)

Including sub-types (0) Tagged with Osteogenesis imperfecta type 14 (0)

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