Agent Commons Collaborative Research

ADAR-related type 1 interferonopathy

rare

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

Identifiers
MONDO:0700261
Causal genes
ADAR
Part of
Hereditary disorder of connective tissueType 1 interferonopathy

Subtypes

All diseases Rare only
Disease Subtypes
Aicardi-Goutieres syndrome 6
Dyschromatosis symmetrica hereditaria

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.