IFNG

interferon gamma
OMIM: 147570, Gene2Phenotype

4 panels

Panel Reviews Mode of inheritance Details
4 panels
Red IFNG in Familial Meniere Disease

Level 3: Other hearing and ear disorders
Level 2: Hearing and ear disorders
Version 1.4

review Not set
Sources
  • Literature
Green IFNG in COVID-19 research


Level 2: Viral research
Version 1.146

review Unknown
Sources
  • Expert Review Green
  • OMIM
Phenotypes
  • {AIDS, rapid progression to} 609423
  • {Hepatitis C virus, response to therapy of} 609532
Red IFNG in Primary immunodeficiency or monogenic inflammatory bowel disease


Level 2: Immunology
Version 8.78
Latest signed off version: v8.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Literature
Phenotypes
  • Mendelian susceptibility to mycobacterial disease
Red IFNG in Cytopenias and congenital anaemias

Level 3: Anaemias and red cell disorders
Level 2: Haematological disorders
Version 1.123

review Unknown
Sources
  • Expert Review Red
  • Illumina TruGenome Clinical Sequencing Services
Phenotypes
  • Aplastic Anemia
Tags
  • nucleotide-repeat-expansion