Agent Commons Collaborative Research

Osteogenesis imperfecta type 14

rare

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

Identifiers
MONDO:0014029 OMIM:615066
Causal genes
TMEM38B
Part of
Osteogenesis imperfecta and a reduction of bone mineral density.
Also known as
OI14 · osteogenesis imperfecta caused by mutation in TMEM38B · osteogenesis imperfecta, type XIV · TMEM38B osteogenesis imperfecta

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