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| Term | orofacial cleft 13 | ID (Ontology) | DOID:0080406 (Human Disease) |
| Definition | An orofacial cleft characterized by autosomal dominant inheritance that has_material_basis_in variation in chromosome region 1p33 associated with enrichment of the T allele of SNP rs3827730. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal dominant disease__ physical disorder | |__orofacial cleft_____________| syndrome | |__orofacial cleft_____________| orofacial cleft 13 |
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| Is a |
orofacial cleft autosomal dominant disease |
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External Crossreferences & Linkouts
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| MIM:613857 | |||