PRDX3

4 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green PRDX3 in Ataxia and cerebellar anomalies - narrow panel Level 2: Neurology Version 8.72 Latest signed off version: v8.0 (30 Apr 2025) 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 4.7 Latest signed off version: v4.0 (30 Apr 2025)	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 6.447 Latest signed off version: v6.0 (30 Apr 2025) 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 with onset in adulthood Level 2: Neurology Version 8.30 Latest signed off version: v8.0 (30 Apr 2025)	review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green NHS GMS Literature Phenotypes Spinocerebellar ataxia, autosomal recessive 32, OMIM:619862