PanelApp (stage)
  1. Genes and Genomic Entities
  2. CD59

CD59

CD59 molecule (CD59 blood group)
OMIM: 107271, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Green CD59 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Haemolytic anaemia, CD59-mediated, with or without immune-mediated polyneuropathy, MIM# 612300

Green CD59 in Complement Deficiencies


Level 2: Immunological disorders
Version 0.73

Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  review Unknown
    Sources
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    • Expert Review Green

    Green CD59 in Hereditary Neuropathy - complex


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.14

    Component of the following Super Panels:

  • Hereditary Neuropathy_CMT_IsolatedAndComplex
  • Neuromuscular Superpanel
  • Progressive Neurological Conditions

    		•  review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • NHS GMS
    Phenotypes
    • Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy 612300

    Green CD59 in Stroke


    Level 2: Neurology and neurodevelopmental disorders
    Version 1.16

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Hemolytic anemia, CD59-mediated, with or without immune-mediated polyneuropathy MIM#612300

    Green CD59 in Red cell disorders


    Level 2: Haematological disorders
    Version 1.24

    		review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Yorkshire and North East GLH
    • North West GLH
    • NHS GMS
    Phenotypes
    • Haemolytic anaemia, CD59-mediated, with or without immune-mediated polyneuropathy, MIM# 612300