ABCA2

ATP binding cassette subfamily A member 2
OMIM: 600047, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green ABCA2 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review
Phenotypes
  • Intellectual developmental disorder with poor growth and with or without seizures or ataxia, 618808

Green ABCA2 in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review
    • Expert Review Green
    • Literature
    Phenotypes
    • Intellectual developmental disorder with poor growth and with or without seizures or ataxia, 618808

    Green ABCA2 in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Intellectual developmental disorder with poor growth and with or without seizures or ataxia, 618808