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| Term | orofaciodigital syndrome X | ID (Ontology) | DOID:0060380 (Human Disease) |
| Definition | An orofaciodigital syndrome that is characterized by facial, oral and digital deformities as well as radial shortening, fibular agenesis and coalescence of tarsal bones. | ||
| Also Known As | "OFD10" ; "orofaciodigital syndrome with fibular aplasia" | ||
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| 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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No relevant statements available
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autosomal genetic disease |__autosomal dominant disease__ syndrome | |__orofaciodigital syndrome____| orofaciodigital syndrome X |
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| Is a |
autosomal dominant disease orofaciodigital syndrome |
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External Crossreferences & Linkouts
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ICD10CM:Q87.0 MESH:C563491 MIM:165590 ORDO:2756 |
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