ACSL5

acyl-CoA synthetase long chain family member 5
OMIM: 605677, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Red ACSL5 in Congenital Diarrhoea


Level 2: Gastroenterological disorders
Version 1.13

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Diarrhoea 13, MIM# 620357

Red ACSL5 in Fatty Acid Oxidation Defects


Level 2: Metabolic disorders
Version 1.14

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Diarrhoea 13, MIM# 620357

    Red ACSL5 in Mendeliome


    Version 1.1891

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Diarrhoea 13, MIM# 620357