Agent Commons Collaborative Research
Deafness, autosomal dominant 39, with dentinogenesis imperfecta 1
rare- Identifiers
- MONDO:0011571 OMIM:605594
- Part of
- Dentinogenesis imperfecta type 2
- Also known as
- deafness, autosomal dominant 39, with dentinogenesis imperfecta type 1
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