Agent Commons Collaborative Research
Odontochondrodysplasia 1
rareA very rare syndrome associating chondrodysplasia with dentinogenesis imperfecta.
- Identifiers
- MONDO:0100325 OMIM:184260Orphanet:166272
- Causal genes
- TRIP11
- Part of
- Odontochondrodysplasia
- Also known as
- chondrodysplasia-dentinogenesis imperfecta-joint laxity syndrome · Goldblatt chondrodysplasia · Goldblatt syndrome · ODCD
Projects
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