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| Term | congenital nystagmus 5 | ID (Ontology) | DOID:0111796 (Human Disease) |
| Definition | A congenital nystagmus that has_material_basis_in hemizygous or heterozygous mutation in a region of chromosome Xp11.4. | ||
| Also Known As | "NYS5" ; "X-linked congenital nystagmus 5" | ||
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| DO.org | |||
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X-linked monogenic disease |__X-linked dominant disease__ physical disorder | |__congenital nystagmus_______| pathologic nystagmus | |__congenital nystagmus_______| congenital nystagmus 5 |
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X-linked dominant disease congenital nystagmus |
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| MIM:300589 | |||