FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term retinitis pigmentosa 96 ID (Ontology) DOID:0061104 (Human Disease)
Definition A retinitis pigmentosa characterized by difficulty with night vision and progressive visual field constriction beginning as early as the third decade of life, but most patients retain good visual acuity into the seventh decade that has_material_basis_in heterozygous mutation in the SAG gene on chromosome 2q37.
Also Known As "RP96"
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 Genes
 retinitis pigmentosa 96       4
 for disease ribbon | retinitis pigmentosa 96       4
 model of | retinitis pigmentosa 96       4
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
retinal degeneration            |
 |__retinitis pigmentosa________|
                                retinitis pigmentosa 96  4 rec.
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Is a autosomal dominant disease
retinitis pigmentosa
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Synonyms
  • "RP96" EXACT OMO:0003012
Secondary IDs
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MIM:620228