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| Term | brachydactyly type A1D | ID (Ontology) | DOID:0110978 (Human Disease) |
| Definition | A brachydactyly type A1 that has_material_basis_in heterozygous mutation in the BMPR1B gene on chromosome 4q22. | ||
| Also Known As | "BDA1D" | ||
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| DO.org | |||
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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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brachydactyly_______________ autosomal dominant disease__| brachydactyly type A1 |__brachydactyly type A1D 1 rec. |
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| Is a | brachydactyly type A1 | ||
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External Crossreferences & Linkouts
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| MIM:616849 | |||