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Retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene

MedGen UID:
1843288
Concept ID:
C5679609
Disease or Syndrome
Synonym: Retinal ciliopathy due to mutation in RP1 gene
 
Orphanet: ORPHA156168

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • Retinal ciliopathy due to mutation in the retinitis pigmentosa-1 gene

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