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ADAR-related type 1 interferonopathy

MONDO:0700261

Any type 1 interferonopathies in which the cause of the disease is a variation in the ADAR gene. Individuals with variants in ADAR can present with a variety of phenotypes, including Aicardi-Goutieres syndrome and dyschromatosis symmetrica hereditaria.

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

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Where it sits in the disease tree

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Part of

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

Sub-types of ADAR-related type 1 interferonopathy

Dyschromatosis symmetrica hereditaria 1 trial
Aicardi-Goutieres syndrome 6 0 trials

Including sub-types (13) Tagged with ADAR-related type 1 interferonopathy (0)

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