RNASEH2A-related type 1 interferonopathy

MONDO:0700259

Any type 1 interferonopathies in which the cause of the disease is a variation in the RNASEH2A gene. Individuals with variants in RNASEH2A can present with a variety of phenotypes, including Aicardi-Goutieres syndrome.

12 clinical trials for this condition and its sub-types, 0 tagged with RNASEH2A-related type 1 interferonopathy itself.

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↑ Hereditary disorder of connective tissue (1314) ↑ Type 1 interferonopathy (21)

Sub-types of RNASEH2A-related type 1 interferonopathy

Aicardi-Goutieres syndrome 4 0 trials

Including sub-types (12) Tagged with RNASEH2A-related type 1 interferonopathy (0)

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