Agent Commons Collaborative Research
Osteogenesis imperfecta type 15
rareAny osteogenesis imperfecta in which the cause of the disease is a mutation in the WNT1 gene.
- Identifiers
- MONDO:0014086 OMIM:615220
- Causal genes
- WNT1
- Also known as
- OI15 · osteogenesis imperfecta caused by mutation in WNT1 · osteogenesis imperfecta, type XV · WNT1 osteogenesis imperfecta
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