PanelApp
  1. Genes and Genomic Entities
  2. AICDA

AICDA

activation induced cytidine deaminase
OMIM: 605257, Gene2Phenotype

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Green AICDA in Vasculitis


Level 2: Immunological disorders
Version 0.93

0 reviews Unknown
Sources
  • Victorian Clinical Genetics Services
  • Expert Review Green

Red AICDA in Cataract


Level 2: Ophthalmological disorders
Version 0.375

1 review Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
Phenotypes
  • Immunodeficiency with hyper-IgM, type 2 605258

Green AICDA in Inflammatory bowel disease


Level 2: Gastroenterological disorders
Version 0.126

Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  0 reviews Unknown
    Sources
    • Victorian Clinical Genetics Services
    • Expert Review Green

    Green AICDA in Mendeliome


    Version 1.3512

    		2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Immunodeficiency with hyper-IgM, type 2, MIM# 605258

    Green AICDA in Predominantly Antibody Deficiency


    Level 2: Immunological disorders
    Version 1.4

    Component of the following Super Panels:

  • Immunological disorders_SuperPanel

    		•  2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Immunodeficiency with hyper-IgM, type 2, MIM# 605258

    Green AICDA in Genomic newborn screening: BabyScreen+


    Level 2: Screening
    Version 1.140

    		1 review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review
    Phenotypes
    • Immunodeficiency with hyper-IgM, type 2, MIM# 605258
    Tags
    • treatable
    • immunological

    Green AICDA in Nucleotide metabolism disorders


    Level 2: Metabolic disorders
    Version 0.8

    Component of the following Super Panels:

  • Metabolic Disorders Superpanel

    		•  2 reviews BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • hyper-IgM syndrome type 2 MONDO:0011528
    • Disorders of ectonucleotide and nucleic acid metabolism