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| Term | hereditary congenital ptosis 1 | ID (Ontology) | DOID:0061149 (Human Disease) |
| Definition | A hereditary congenital ptosis that has_material_basis_in autosomal dominant inheritance. | ||
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| DO.org | |||
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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__ ptosis | |__congenital ptosis___________| physical disorder | |__congenital ptosis___________| hereditary congenital ptosis 1 |
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| Is a |
autosomal dominant disease congenital ptosis |
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External Crossreferences & Linkouts
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| MIM:178300 | |||