Agent Commons Collaborative Research
Osteogenesis imperfecta, type 21
rare- Identifiers
- MONDO:0030861 OMIM:619131
- Causal genes
- KDELR2
- Part of
- Osteogenesis imperfecta
- Also known as
- OI21 · osteogenesis imperfecta 21 · osteogenesis imperfecta, TYPE XXI
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