osteogenesis imperfecta type 16 (Q27674944)
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osteogenesis imperfecta that has material basis in contiguous gene deletion on chromosome 11p11
- OI16
- chromosome 11p11.2 deletion syndrome 91.3-KB
- osteogenesis imperfecta type XVI
- Chromosome 11P11.2 Deletion Syndrome, 91.3-Kb
- OSTEOGENESIS IMPERFECTA, TYPE XVI; OI16
- OSTEOGENESIS IMPERFECTA, TYPE XVI
- Oi, Type 16
Language | Label | Description | Also known as |
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English | osteogenesis imperfecta type 16 |
osteogenesis imperfecta that has material basis in contiguous gene deletion on chromosome 11p11 |
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