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| Term | orofacial cleft 14 | ID (Ontology) | DOID:0080407 (Human Disease) |
| Definition | An orofacial cleft that is characterized by incomplete median clefts of both the lower lip and upper lip, double labial frenulum and fusion of the upper gingival and upper labial mucosa, in addition to poor dental alignment, and increased interdental distance between the lower and upper median incisors. | ||
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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 recessive disease__ physical disorder | |__orofacial cleft______________| syndrome | |__orofacial cleft______________| orofacial cleft 14 |
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| Is a |
orofacial cleft autosomal recessive disease |
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External Crossreferences & Linkouts
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| MIM:615892 | |||