PEX11A

peroxisomal biogenesis factor 11 alpha
OMIM: 603866, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red PEX11A in Malformations of cortical development

Level 3: Neurodevelopmental disorders
Level 2: Neurology and neurodevelopmental disorders
Version 4.26
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Cerebral malformation
  • review Unknown
    Sources
    • Literature
    Phenotypes
    • Zellweger syndrome
    • peroxisome proliferation
    • mild peroxisomal biogenesis defect
    Tags
    • watchlist
    Red PEX11A in Undiagnosed metabolic disorders

    Level 3: Specific metabolic abnormalities
    Level 2: Metabolic disorders
    Version 1.617

    review Unknown
    Sources
    • Literature
    Phenotypes
    • Zellweger syndrome
    • peroxisome proliferation
    • mild peroxisomal biogenesis defect
    Tags
    • watchlist
    Red PEX11A in Likely inborn error of metabolism - targeted testing not possible


    Version 4.137
    Latest signed off version: v4.0 (22 Mar 2023)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood
  • review Unknown
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Zellweger syndrome
    • peroxisome proliferation
    • mild peroxisomal biogenesis defect