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| Term | cataract 40 | ID (Ontology) | DOID:0110272 (Human Disease) |
| Definition | A cataract that has_material_basis_in mutation in the NHS gene on chromosome Xp22. | ||
| Also Known As | "cataract 40 with or without microcornea" ; "cataract 40 X-linked" ; "CTRCT40" | ||
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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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monogenic disease |__X-linked monogenic disease__ |__cataract____________________| lens disease | |__cataract____________________| cataract 40 1 rec. |
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| Is a |
X-linked monogenic disease cataract |
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External Crossreferences & Linkouts
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ICD10CM:Q12.0 MIM:302200 |
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