FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term retinitis pigmentosa 7 ID (Ontology) DOID:0110383 (Human Disease)
Definition A retinitis pigmentosa that has_material_basis_in mutation in the PRPH2 gene on chromosome 6p21.
Also Known As "RP7"
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 Genes
 retinitis pigmentosa 7       5
 for disease ribbon | retinitis pigmentosa 7       5
 model of | retinitis pigmentosa 7       5
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease___
 |__autosomal recessive disease__|
polygenic disease                |
 |__digenic disease______________|
retinal degeneration             |
 |__retinitis pigmentosa_________|
                                 retinitis pigmentosa 7  5 rec.
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Is a autosomal dominant disease
autosomal recessive disease
digenic disease
retinitis pigmentosa
Part of
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Synonyms
  • "RP7" EXACT OMO:0003012
Secondary IDs
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ICD10CM:H35.5
MESH:C564284
MIM:608133