Aicardi-Goutieres syndrome Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An autosomal recessive disease that is a genetically heterogeneous encephalopathy characterized in its most severe form by cerebral atrophy, leukodystrophy, intracranial calcifications, chronic cerebrospinal fluid (CSF) lymphocytosis, increased CSF alpha-interferon, and negative serologic investigations for common prenatal infections. (Human Disease Ontology, DOID_0050629)
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5 genes/proteins associated with the disease Aicardi-Goutieres syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
RNASEH2B ribonuclease H2, subunit B 2.88009
SAMHD1 SAM domain and HD domain 1 2.88009
IFIH1 interferon induced with helicase C domain 1 2.88009
TREX1 three prime repair exonuclease 1 2.88009
ADAR adenosine deaminase, RNA-specific 2.88009