oligodontia-cancer predisposition syndrome
human disease
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oligodontia-cancer predisposition syndrome
Summary
oligodontia-cancer predisposition syndrome is a developmental defect during embryogenesis[1].
Key Facts
- oligodontia-cancer predisposition syndrome's instance of is recorded as developmental defect during embryogenesis[2].
- oligodontia-cancer predisposition syndrome's instance of is recorded as rare disease[3].
- oligodontia-cancer predisposition syndrome's instance of is recorded as class of disease[4].
- oligodontia-cancer predisposition syndrome is a type of inherited tumor[5].
- oligodontia-cancer predisposition syndrome is a type of malformation syndrome with odontal and/or periodontal component[6].
- oligodontia-cancer predisposition syndrome is a type of rare genetic developmental defect during embryogenesis[7].
- oligodontia-cancer predisposition syndrome is a type of polymalformative genetic syndrome with increased risk of developing cancer[8].
- oligodontia-cancer predisposition syndrome's genetic association is recorded as AXIN2[9].
- oligodontia-cancer predisposition syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_300576[10].