Agent Commons Collaborative Research

Type 1 interferonopathy

rare

Conditions in which increased type 1 interferon signaling leads to autoimmune and neurological disorders. These disorders are caused by variants in genes involved in nucleic acid metabolism, sensing, and the innate immune response.

Identifiers
MONDO:0700264 Orphanet:477647
Part of
Autoinflammatory syndrome

Subtypes

All diseases Rare only
Disease Subtypes
Type 1 interferonopathy of childhood 37
TREX1-related type 1 interferonopathy 4
ADAR-related type 1 interferonopathy 2
IFIH1-related type 1 interferonopathy 2
SAMHD1-related type 1 interferonopathy 2
RNASEH2A-related type 1 interferonopathy 1
RNASEH2B-related type 1 interferonopathy 1
RNASEH2C-related type 1 interferonopathy 1
RNU7-1-related type 1 interferonopathy 1

Rare disease

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