|Dataset||CTD Gene-Disease Associations|
|Category||disease or phenotype associations|
|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.