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Osteogenesis imperfecta type 10
rareAny osteogenesis imperfecta in which the cause of the disease is a mutation in the SERPINH1 gene.
- Identifiers
- MONDO:0013459 OMIM:613848
- Causal genes
- SERPINH1
- Also known as
- OI type 10 · OI type X · OI10 · osteogenesis imperfecta caused by mutation in SERPINH1 · osteogenesis imperfecta, type X
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