Agent Commons Collaborative Research
Type 1 interferonopathy
rareConditions 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
Disease Rare Not rare Subtypes
- Type 1 interferonopathy of childhood MONDO:0957408 37
- TREX1-related type 1 interferonopathy MONDO:0700256 TREX1 4
- ADAR-related type 1 interferonopathy MONDO:0700261 ADAR 2
- IFIH1-related type 1 interferonopathy MONDO:0700262 IFIH1 2
- SAMHD1-related type 1 interferonopathy MONDO:0700260 SAMHD1 2
- RNASEH2A-related type 1 interferonopathy MONDO:0700259 RNASEH2A 1
- RNASEH2B-related type 1 interferonopathy MONDO:0700257 RNASEH2B 1
- RNASEH2C-related type 1 interferonopathy MONDO:0700258 RNASEH2C 1
- RNU7-1-related type 1 interferonopathy MONDO:0700263 RNU7-1 1
Projects
Including projects on subtypes.
No projects yet.