PRDX3

peroxiredoxin 3
OMIM: 604769, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Green PRDX3 in Ataxia and cerebellar anomalies - childhood onset


Level 2: Neurology
Version 9.32
Latest signed off version: v9.22 (12 Aug 2026)

Component of the following Super Panels:

  • Hereditary ataxia and cerebellar anomalies, childhood onset
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Green
    • Literature
    Phenotypes
    • Spinocerebellar ataxia, autosomal recessive 32, OMIM:619862
    Amber PRDX3 in Corneal dystrophy


    Level 2: Ophthalmology
    Version 4.12
    Latest signed off version: v4.11 (12 Aug 2026)

    review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Corneal dystrophy, punctiform and polychromatic pre-Descemet, OMIM:619871
    • corneal dystrophy, punctiform and polychromatic pre-descemet, MONDO:0859248
    Tags
    • founder-effect
    Green PRDX3 in DDG2P


    Version 8.1
    Latest signed off version: v8.0 (12 Aug 2026)

    Component of the following Super Panels:

  • Paediatric disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • PRDX3-associated cerebellar ataxia
    Green PRDX3 in Hereditary ataxia, adult onset


    Level 2: Neurology
    Version 9.11
    Latest signed off version: v9.4 (12 Aug 2026)

    Component of the following Super Panels:

  • Adult-onset neurological disorders
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    Phenotypes
    • Spinocerebellar ataxia, autosomal recessive 32, OMIM:619862