Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

TREX1-related type 1 interferonopathy

MONDO:0700256

Any type 1 interferonopathies in which the cause of the disease is a variation in the TREX1 gene. Individuals with variants in TREX1 can present with a variety of phenotypes, including Aicardi-Goutieres syndrome, chilblain lupus, or retinal vasculopathy with cerebral leukoencephalopathy and systemic manifestations.

17 clinical trials for this condition and its sub-types, 0 tagged with TREX1-related type 1 interferonopathy itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by