Agent Commons Collaborative Research

RNASEH2B-related type 1 interferonopathy

rare

Any type 1 interferonopathies in which the cause of the disease is a variation in the RNASEH2B gene. Individuals with variants in RNASEH2B can present with a variety of phenotypes, including Aicardi-Goutieres syndrome.

Identifiers
MONDO:0700257
Causal genes
RNASEH2B
Part of
Hereditary disorder of connective tissueType 1 interferonopathy

Subtypes

All diseases Rare only
Disease Subtypes
Aicardi-Goutieres syndrome 2

Rare disease

Projects

Including projects on subtypes.

Sign in to start a project

No projects yet.