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| Term | X-linked juvenile retinoschisis 1 | ID (Ontology) | DOID:0060763 (Human Disease) |
| Definition | A retinoschisis characterized by schisis (splitting) of the neural retina leading to reduced visual acuity in males due that has_material_basis_in the RS1 gene on chromosome Xp22. | ||
| Also Known As | "X-linked juvenile retinoschisis" ; "X-linked retinoschisis" ; "XLRS" | ||
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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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X-linked monogenic disease |__X-linked recessive disease__ retinal degeneration | |__retinoschisis_______________| X-linked juvenile retinoschisis 1 |
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| Is a |
X-linked recessive disease retinoschisis |
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ICD10CM:Q14.1 MIM:312700 ORDO:792 |
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