1. Genes and Genomic Entities
  2. CYP2C8

CYP2C8

cytochrome P450 family 2 subfamily C member 8
OMIM: 601129, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Red CYP2C8 in Rhabdomyolysis and metabolic muscle disorders

Level 3: Neuromuscular disorders
Level 2: Neurology and neurodevelopmental disorders
Version 3.48
Latest signed off version: v3.0 (22 Mar 2023)

Component of the following Super Panels:

  • Hypotonic infant
  • Other rare neuromuscular disorders

    		•  review Unknown
    Sources
    • Radboud University Medical Center, Nijmegen
    Phenotypes
    • {Drug metabolism, altered, CYP2C8-related}, OMIM:618018
    • Rhabdomyolysis, cerivastatin-induced
    Tags
    • pharmacogenetics
    Red CYP2C8 in Other rare neuromuscular disorders


    Version 19.202
    Latest signed off version: v19.1 (22 Mar 2023)

    		review Unknown
    Sources
    • Expert Review Red
    Phenotypes
    • Rhabdomyolysis, cerivastatin-induced
    Red CYP2C8 in Acute rhabdomyolysis

    Level 3: Neuromuscular disorders
    Level 2: Neurology and neurodevelopmental disorders
    Version 1.18
    Latest signed off version: v1.7 (31 May 2023)

    		review Unknown
    Sources
    • NHS GMS
    • Expert Review Red
    Phenotypes
    • Rhabdomyolysis, cerivastatin-induced
    • {Drug metabolism, altered, CYP2C8-related}, OMIM:618018
    Tags
    • to_be_confirmed_NHSE