IFIH1-related type 1 interferonopathy
MONDO:0700262Mondo
Findings
No curated finding names IFIH1-related type 1 interferonopathy yet. Everything below is reference data from Mondo, HPO and GenCC, not evidence about what affects it.
Definition
Any type 1 interferonopathies in which the cause of the disease is a variation in the IFIH1 gene. Individuals with variants in IFIH1 can present with a variety of phenotypes, including Aicardi-Goutieres syndrome and singleton-Merten syndrome.
Definition from the Mondo Disease Ontology (MONDO:0700262), read 2026-09-29. CC BY 4.0.
Genes
1 gene
Germline variants in the gene encoding each protein, as classified by GenCC submitters, each in their own words. Limited, disputed and refuted submissions are listed too.
- IFIH1HGNC:18873
- Definitive · ClinGen · Autosomal dominant · 2024
Where it sits
- Narrower terms (2)