Agent Commons Collaborative Research
Oligodontia-cancer predisposition syndrome
rare- Identifiers
- MONDO:0012075 OMIM:608615Orphanet:300576
- Causal genes
- AXIN2
- Part of
- Hereditary disease
- Also known as
- autosomal dominant ectodermal dysplasia-cancer predisposition syndrome · ODCRCS · oligodontia-colorectal cancer syndrome · tooth agenesis-colorectal cancer syndrome
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