FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term retinitis pigmentosa 97 ID (Ontology) DOID:0061110 (Human Disease)
Definition A retinitis pigmentosa characterized by onset of night blindness and visual field defects in the first decade of life, with later onset of reduced visual acuity that has_material_basis_in heterozygous mutation in the VWA8 gene on chromosome 13q14.
Also Known As "RP97"
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 Genes
 retinitis pigmentosa 97       1
 for disease ribbon | retinitis pigmentosa 97       1
 model of | retinitis pigmentosa 97       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
retinal degeneration            |
 |__retinitis pigmentosa________|
                                retinitis pigmentosa 97  1 rec.
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Is a autosomal dominant disease
retinitis pigmentosa
Part of
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Synonyms
  • "RP97" EXACT OMO:0003012
Secondary IDs
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MIM:620422