NCF4

neutrophil cytosolic factor 4
OMIM: 601488, Gene2Phenotype

7 panels

Panel Reviews Mode of inheritance Details
7 panels

Green NCF4 in Vasculitis


Level 2: Immunological disorders
Version 0.82

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type III MIM#613960

Red NCF4 in Cataract


Level 2: Ophthalmological disorders
Version 0.366

review Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services

Green NCF4 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type III MIM#613960

Green NCF4 in Phagocyte Defects


Level 2: Immunological disorders
Version 1.29

Component of the following Super Panels:

  • Immunological disorders_SuperPanel
  • review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    • Melbourne Genomics Health Alliance Immunology Flagship
    • Victorian Clinical Genetics Services
    Phenotypes
    • Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type III MIM#613960

    Green NCF4 in Chronic granulomatous disease


    Level 2: Immunological disorders
    Version 1.3

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • Expert list
    Phenotypes
    • Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type III MIM#613960

    Red NCF4 in Additional findings_Paediatric


    Level 2: Screening
    Version 0.278

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Red
    • BabySeq Category C gene
    Phenotypes
    • Chronic granulomatous disease

    Green NCF4 in BabyScreen+ newborn screening


    Level 2: Screening
    Version 1.113

    review BIALLELIC, autosomal or pseudoautosomal
    Sources
    • Expert Review Green
    • BabySeq Category C gene
    • BeginNGS
    Phenotypes
    • Granulomatous disease, chronic, autosomal recessive, cytochrome b-positive, type III MIM#613960
    Tags
    • treatable
    • immunological