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| Term | syndactyly type 3 | ID (Ontology) | DOID:0111817 (Human Disease) |
| Definition | A syndactyly characterized by complete and bilateral syndactyly between the 4th and 5th fingers that has_material_basis_in heterozygous mutation in the GJA1 gene on chromosome 6q22.31. | ||
| Also Known As | "ringand little finger syndactyly" ; "SDTY3" ; "syndactyly of fingers 4 and 5" (for all, see Synonyms field below) | ||
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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__ synostosis | |__syndactyly__________________| syndactyly type 3 |
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| Is a |
autosomal dominant disease syndactyly |
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Synonyms & Secondary IDs
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External Crossreferences & Linkouts
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GARD:5088 MESH:C538154 MIM:186100 ORDO:93404 SNOMEDCT_US_2023_03_01:715725001 UMLS_CUI:C1861366 |
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