G6PD

glucose-6-phosphate dehydrogenase
OMIM: 305900, Gene2Phenotype

12 panels

Panel Reviews Mode of inheritance Details
12 panels

Red G6PD in Hydrops fetalis


Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.313

review X-LINKED: hemizygous mutation in males, biallelic mutations in females
Sources
  • Expert Review Red
  • Expert list
Phenotypes
  • Hemolytic anemia, G6PD deficient (favism), MIM# 300908

Green G6PD in Mendeliome


Version 1.1891

review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Haemolytic anaemia, G6PD deficient (favism), MIM# 300908

Green G6PD in Phagocyte Defects


Level 2: Immunological disorders
Version 1.29

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Hemolytic anemia, G6PD deficient (favism), MIM# 300908

    Amber G6PD in Pulmonary Arterial Hypertension


    Level 2: Cardiovascular disorders
    Version 1.39

    review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Pulmonary arterial hypertension

    Green G6PD in Chronic granulomatous disease


    Level 2: Immunological disorders
    Version 1.3

    review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Hemolytic anemia, G6PD deficient (favism) MIM#300908

    Green G6PD in Pharmacogenomics_Paediatric


    Level 2: Screening
    Version 0.50

    review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Haemolytic anemia, G6PD deficient (favism), MIM# 300908

    Green G6PD in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • BabySeq Category A gene
    • Expert Review Green
    Phenotypes
    • Glucose-6-phosphate dehydrogenase deficiency

    Green G6PD in Red cell disorders


    Level 2: Haematological disorders
    Version 1.24

    review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
    Sources
    • Expert Review Green
    • Yorkshire and North East GLH
    • NHS GMS
    • Wessex and West Midlands GLH
    • North West GLH
    • London South GLH
    Phenotypes
    • Haemolytic anaemia, G6PD deficient (favism), MIM# 300908

    Red G6PD in Fetal anomalies


    Version 1.255

    review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Haemolytic anaemia, G6PD deficient (300908)

    Red G6PD in Prepair 1000+


    Level 2: Screening
    Version 1.9

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Red
    • Literature
    Phenotypes
    • Haemolytic anaemia, G6PD deficient (favism) (MIM#300908)

    Green G6PD in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.113

    review X-LINKED: hemizygous mutation in males, biallelic mutations in females
    Sources
    • Expert Review Green
    • BabySeq Category A gene
    • BeginNGS
    Phenotypes
    • Glucose-6-phosphate dehydrogenase deficiency, MIM#300908
    Tags
    • treatable
    • haematological

    Green G6PD in Transplant Co-Morbidity Superpanel


    Level 2: Screening
    Version 0.18

    review X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
    Sources
    • Expert Review Green
    Phenotypes
    • Haemolytic anaemia