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| Term | optic atrophy 2 | ID (Ontology) | DOID:0111443 (Human Disease) |
| Definition | An optic atrophy that has_material_basis_in variation in a region on chromosome Xp11.4-p11.21. | ||
| Also Known As | "OPA2" ; "X-linked optic atrophy 2" | ||
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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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optic nerve disease |__optic atrophy |__optic atrophy 2 |
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| Is a | optic atrophy | ||
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| MIM:311050 | |||