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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.

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Part of

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

Sub-types of IFIH1-related type 1 interferonopathy

Including sub-types (12) Tagged with IFIH1-related type 1 interferonopathy (0)
Trials to join now! 8 Not yet recruiting 1 Not yet finished but already full! 1 Completed 2
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