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| Term | retinitis pigmentosa 88 | ID (Ontology) | DOID:0112145 (Human Disease) |
| Definition | A retinitis pigmentosa characterized by night blindness and constriction of peripheral visual fields, with mildly reduced visual acuity that has_material_basis_in homozygous or compound heterozygous mutation in the RP1L1 gene on chromosome 8p23.1. | ||
| Also Known As | "RP88" | ||
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autosomal genetic disease |__autosomal recessive disease__ retinal degeneration | |__retinitis pigmentosa_________| retinitis pigmentosa 88 |
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| Is a |
autosomal recessive disease retinitis pigmentosa |
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| MIM:618826 | |||