| General Information | |||
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| Term | orofacial cleft 5 | ID (Ontology) | DOID:0080399 (Human Disease) |
| Definition | An orofacial cleft that has_material_basis_in mutation in the MSX1 gene on chromosome 4p16. | ||
| Also Known As | "nonsyndromic cleft lip with or without cleft palate 5" | ||
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| DO.org | |||
| Annotations | |||
| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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physical disorder__ syndrome___________| orofacial cleft |__orofacial cleft 5 2 rec. |
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| Parents/Children View Depth |
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Relationships
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| Is a | orofacial cleft | ||
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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MESH:C563843 MIM:608874 |
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