Browse
Explore conditions, clinical trials, and the organisations running them.
Up to: Hereditary disorder of connective tissue · Type 1 interferonopathy
IFIH1-related type 1 interferonopathy
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.
-
Aicardi-Goutieres syndrome 7 0 trials
-
Singleton-Merten syndrome 1 0 trials