FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term retinitis pigmentosa 30 ID (Ontology) DOID:0110406 (Human Disease)
Definition A retinitis pigmentosa that has_material_basis_in mutation in the FSCN2 gene on chromosome 17q25.
Also Known As "RP30"
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 Genes
 retinitis pigmentosa 30       1
 for disease ribbon | retinitis pigmentosa 30       1
 model of | retinitis pigmentosa 30       1
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  retinal degeneration
   |__retinitis pigmentosa
       |__retinitis pigmentosa 30  1 rec.
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Is a retinitis pigmentosa
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Synonyms
  • "RP30" EXACT OMO:0003012
Secondary IDs
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ICD10CM:H35.5
MESH:C564310
MIM:607921