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| Term | retinitis pigmentosa 92 | ID (Ontology) | DOID:0061107 (Human Disease) | |||||||||
| Definition | A retinitis pigmentosa characterized by relatively mild disease, with onset of night blindness and vision loss in the third to sixth decades of life that has_material_basis_in homozygous mutation in the HKDC1 gene on chromosome 10q22. | |||||||||||
| Also Known As | "RP92" | |||||||||||
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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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autosomal genetic disease |__autosomal recessive disease__ retinal degeneration | |__retinitis pigmentosa_________| retinitis pigmentosa 92 1 rec. |
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| Is a |
autosomal recessive disease retinitis pigmentosa |
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External Crossreferences & Linkouts
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| MIM:619614 | |||