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| Term | cone-rod dystrophy 18 | ID (Ontology) | DOID:0111024 (Human Disease) |
| Definition | A cone-rod dystrophy that has_material_basis_in homozygous mutation in the RAB28 gene on chromosome 4p15. | ||
| Also Known As | "CORD18" | ||
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| DO.org | |||
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monogenic disease_____ retinal degeneration__| cone-rod dystrophy |__cone-rod dystrophy 18 |
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| Is a | cone-rod dystrophy | ||
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| MIM:615374 | |||