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Up to: Hereditary disorder of connective tissue · Type 1 interferonopathy
TREX1-related type 1 interferonopathy
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.
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Aicardi-Goutieres syndrome 1 2 trials Sub-types →
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Chilblain lupus 1 0 trials