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| Term | Tukel syndrome | ID (Ontology) | DOID:0081021 (Human Disease) |
| Definition | A congenital fibrosis of the extraocular muscles that is characterized by nonprogressive restrictive ophthalmoplegia with blepharoptosis of the right eye and postaxial oligodactyly/oligosyndactyly of the hands, with the right more severely affected than the left. | ||
| Also Known As | "congenital fibrosis of the extraocular muscles 4" | ||
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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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No relevant statements available
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autosomal genetic disease |__autosomal recessive disease_____________________ physical disorder | |__congenital fibrosis of the extraocular muscles__| ocular motility disease | |__congenital fibrosis of the extraocular muscles__| Tukel syndrome |
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| Is a |
autosomal recessive disease congenital fibrosis of the extraocular muscles |
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External Crossreferences & Linkouts
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GARD:9814 MESH:C536925 MIM:609428 |
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