GAA

glucosidase alpha, acid
OMIM: 606800, Gene2Phenotype

14 panels

Panel Reviews Mode of inheritance Details
14 panels

Green GAA in Glycogen Storage Diseases


Level 2: Metabolic disorders
Version 1.3

Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Glycogen storage disease II (MIM#232300)
    • MONDO:0009290

    Red GAA in Hypertrophic cardiomyopathy_HCM


    Level 2: Cardiovascular disorders
    Version 1.10

    Component of the following Super Panels:

  • Adult Cardiac SuperPanel
  • Cardiomyopathy_Adult_SuperPanel
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • Victorian Clinical Genetics Services
    Phenotypes
    • Glycogen storage disease II, MIM#232300

    Green GAA in Mendeliome


    Version 1.3512

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Glycogen storage disease II, MIM# 232300
    • MONDO:0009290

    Green GAA in Lysosomal Storage Disorder


    Level 2: Metabolic conditions
    Version 1.23

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel
  • Progressive Neurological Conditions
  • 1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Glycogen storage disease II, MIM# 232300
    • MONDO:0009290

    Green GAA in Additional findings_Adult


    Level 2: Screening
    Version 1.130

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Glycogen storage disease II 232300
    • Pompe disease

    Green GAA in Limb-Girdle Muscular Dystrophy and Distal Myopathy


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.63

    Component of the following Super Panels:

  • Myopathy Superpanel
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • 3 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Glycogen storage disease II 232300

    Green GAA in Rhabdomyolysis and Metabolic Myopathy


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.26

    Component of the following Super Panels:

  • Myopathy Superpanel
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions
  • 2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Royal Melbourne Hospital
    Phenotypes
    • Glycogen storage disease II (MIM#232300)

    Green GAA in Mackenzie's Mission_Reproductive Carrier Screening


    Level 2: Screening
    Version 0.110

    0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Glycogen storage disease II, 232300 (3)

    Green GAA in Cardiomyopathy_Paediatric


    Level 2: Cardiovascular disorders
    Version 0.207

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • South West GLH
    • NHS GMS
    • Expert Review Green
    • MetBioNet
    • London South GLH
    Phenotypes
    • HCM, mixed
    • Glycogen storage disease II, 232300
    • syndromic HCM
    • Hypotonia, muscle weakness, progressive respiratory failure
    • Glycogen storage disease type II (Pompe disease)

    Green GAA in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    0 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • BabySeq Category A gene
    • Expert Review Green
    Phenotypes
    • Glycogen storage disease II

    Green GAA in Fetal anomalies


    Version 1.465

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Genomics England PanelApp
    Phenotypes
    • Glycogen storage disease II MIM#232300

    Green GAA in Prepair 1000+


    Level 2: Screening
    Version 2.14

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Glycogen storage disease II (Pompe disease), 232300

    Green GAA in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.140

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BabySeq Category A gene
    • BeginNGS
    Phenotypes
    • Glycogen storage disease II, Pompe disease, MIM# 232300
    Tags
    • treatable
    • metabolic

    Green GAA in Prepair 500+


    Level 2: Screening
    Version 2.0

    1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Mackenzie's Mission
    Phenotypes
    • Glycogen storage disease II, MIM#232300