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General Information
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| Term |
congenital fibrosis of the extraocular muscles 1 |
ID (Ontology) |
DOID:0081015 (Human Disease) |
| Definition |
A congenital fibrosis of the extraocular muscles that is characterized by bilateral blepharoptosis and ophthalmoplegia with the eyes fixed in an infraducted position about 20 to 30 degrees below the horizontal midline and that has_material_basis_in heterozygous mutation in the KIF21A gene on chromosome 12q12. |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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No relevant records available
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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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| Full annotation statements | Relevant FlyBase reports |
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| Genes |
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congenital fibrosis of the extraocular muscles 1 | 1 | for disease ribbon | congenital fibrosis of the extraocular muscles 1 | 1 | model of | congenital fibrosis of the extraocular muscles 1 | 1 |
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