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| Term | orofacial cleft 7 | ID (Ontology) | DOID:0080400 (Human Disease) |
| Definition | An orofacial cleft that has_material_basis_in by homozygous mutation in the PVRL1 gene on chromosome 11q23. | ||
| Also Known As | "Zlotogora-Ogur syndrome" | ||
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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 7 |
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| Is a |
orofacial cleft autosomal recessive disease |
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| MESH:C563464 | |||