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| Term | retinitis pigmentosa 86 | ID (Ontology) | DOID:0112143 (Human Disease) |
| Definition | A retinitis pigmentosa characterized by night blindness followed by progressive narrowing of visual fields and decline in visual acuity that has_material_basis_in mutation in the KIAA1549 gene on chromosome 7q34. | ||
| Also Known As | "RP86" | ||
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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 |__autosomal genetic disease__ retinal degeneration | |__retinitis pigmentosa_______| retinitis pigmentosa 86 |
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| Is a |
autosomal genetic disease retinitis pigmentosa |
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| MIM:618613 | |||