PDHB

pyruvate dehydrogenase E1 beta subunit
OMIM: 179060, Gene2Phenotype

9 panels

Panel Reviews Mode of inheritance Details
9 panels

Green PDHB in Pyruvate dehydrogenase (PDH) deficiency


Version 1.31
Latest signed off version: v1.2 (17 Feb 2020)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • NHS GMS
  • Expert Review Green
Phenotypes
  • PYRUVATE DEHYDROGENASE E1-BETA DEFICIENCY OMIM:614111
  • pyruvate dehydrogenase E1-beta deficiency MONDO:0013580

Green PDHB in Undiagnosed metabolic disorders

Level 3: Specific metabolic abnormalities
Level 2: Metabolic disorders
Version 1.542

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Pyruvate dehydrogenase E1? subunit deficiency (Disorders of pyruvate metabolism)
  • Pyruvate dehydrogenase E1-beta deficiency, 614111

Green PDHB in Inborn errors of metabolism


Version 2.263
Latest signed off version: v2.3 (17 Feb 2020)

Component of the following Super Panels:

  • Hypotonic infant
  • Paediatric disorders
  • White matter disorders - childhood onset
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • London North GLH
    • NHS GMS
    • Expert Review Green
    Phenotypes
    • Pyruvate dehydrogenase E1? subunit deficiency (Disorders of pyruvate metabolism)
    • Pyruvate dehydrogenase E1-beta deficiency, 614111

    Green PDHB in Possible mitochondrial disorder - nuclear genes


    Version 1.94
    Latest signed off version: v1.17 (11 Nov 2020)

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • NHS GMS
    • Expert Review Green
    Phenotypes
    • PYRUVATE DEHYDROGENASE E1-BETA DEFICIENCY, 614111

    Red PDHB in Fetal anomalies


    Version 1.900
    Latest signed off version: v1.92 (21 Aug 2020)

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Literature
    Phenotypes
    • Pyruvate dehydrogenase E1-beta deficiency, 614111

    Green PDHB in Intellectual disability

    Level 3: Neurodevelopmental disorders
    Level 2: Neurology and neurodevelopmental disorders
    Version 3.1659
    Latest signed off version: v3.2 (13 Feb 2020)

    Component of the following Super Panels:

  • Hypotonic infant
  • Paediatric disorders
  • White matter disorders - childhood onset
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Pyruvate dehydrogenase E1-beta deficiency, MIM#614111

    Green PDHB in Mitochondrial disorders

    Level 3: Mitochondrial
    Level 2: Metabolic disorders
    Version 2.117
    Latest signed off version: v2.4 (17 Feb 2020)

    Component of the following Super Panels:

  • White matter disorders - childhood onset
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green
    • Radboud University Medical Center, Nijmegen
    Phenotypes
    • Pyruvate dehydrogenase E1-beta deficiency, 614111

    Red PDHB in Childhood onset dystonia or chorea or related movement disorder


    Version 1.241
    Latest signed off version: v1.137 (5 Aug 2021)

    review Not set
    Sources
    • Expert Review Red
    • London North GLH

    Green PDHB in Severe Paediatric Disorders


    Version 1.127

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Next Generation Children Project
    • Expert Review Green
    • Expert list
    Phenotypes
    • Pyruvate dehydrogenase E1-beta deficiency, 614111