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| General Information | |||
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| Term | retinitis pigmentosa 6 | ID (Ontology) | DOID:0110413 (Human Disease) |
| Definition | A retinitis pigmentosa that has_material_basis_in variation in the chromosome region Xp21.3-p21.2. | ||
| Also Known As | "RP6" | ||
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| DO.org | |||
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| Records annotated with this term OR any of its CHILD TERMS | |||
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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No relevant statements available
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retinal degeneration |__retinitis pigmentosa |__retinitis pigmentosa 6 |
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| Is a | retinitis pigmentosa | ||
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External Crossreferences & Linkouts
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ICD10CM:H35.5 MESH:C564065 MIM:312612 |
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