IFIH1-related type 1 interferonopathy

MONDO:0700262

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.

12 clinical trials for this condition and its sub-types, 0 tagged with IFIH1-related type 1 interferonopathy itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →

Part of

↑ Hereditary disorder of connective tissue (1311) ↑ Type 1 interferonopathy (21)

Sub-types of IFIH1-related type 1 interferonopathy

Aicardi-Goutieres syndrome 7 0 trials
Singleton-Merten syndrome 1 0 trials

Including sub-types (12) Tagged with IFIH1-related type 1 interferonopathy (0)

We haven't found any trials for this condition yet. Follow it to get notified when new trials appear.