SAMHD1-related type 1 interferonopathy

MONDO:0700260

Any type 1 interferonopathies in which the cause of the disease is a variation in the SAMHD1 gene. Individuals with variants in SAMHD1 can present with a variety of phenotypes, including Aicardi-Goutieres syndrome and chilblain lupus.

12 clinical trials for this condition and its sub-types, 0 tagged with SAMHD1-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 SAMHD1-related type 1 interferonopathy

Aicardi-Goutieres syndrome 5 0 trials
Chilblain lupus 2 0 trials

Including sub-types (12) Tagged with SAMHD1-related type 1 interferonopathy (0)

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