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| Term | syndactyly type 1 | ID (Ontology) | DOID:0111816 (Human Disease) |
| Definition | A syndactyly characterized by complete or partial webbing between the third and fourth fingers and/or the second and third toes that has_material_basis_in heterozygous duplication of a region of chromosome 2q34-q36. | ||
| Also Known As | "chromosome 2q35 duplication syndrome" ; "SDTY1" ; "syndactyly, type 1, with or without craniosynostosis" | ||
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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 dominant disease________ chromosomal disease | |__chromosomal duplication syndrome__| synostosis | |__syndactyly________________________| syndactyly type 1 |
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| Is a |
autosomal dominant disease chromosomal duplication syndrome syndactyly |
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External Crossreferences & Linkouts
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GARD:5081 MIM:185900 ORDO:93402 |
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