NOD2

nucleotide binding oligomerization domain containing 2
OMIM: 605956, Gene2Phenotype

5 panels

Panel Reviews Mode of inheritance Details
5 panels

Red NOD2 in Vasculitis


Level 2: Immunological disorders
Version 0.82

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Blau syndrome, MIM# 186580

Green NOD2 in Inflammatory bowel disease


Level 2: Gastroenterological disorders
Version 0.121

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review
    Phenotypes
    • {Inflammatory bowel disease 1, Crohn disease} 266600
    • {Yao syndrome} 617321

    Green NOD2 in Mendeliome


    Version 1.1891

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Blau syndrome, MIM# 186580

    Green NOD2 in Systemic Autoinflammatory Disease_Periodic Fever


    Level 2: Immunological disorders
    Version 1.47

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Blau syndrome, MIM# 186580

    Green NOD2 in Chronic granulomatous disease


    Level 2: Immunological disorders
    Version 1.3

    review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Blau syndrome MIM#186580
    • granulomatous disease