| Dataset | DISEASES Curated Gene-Disease Association Evidence Scores |
| 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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7 genes involed in the disease aicardi-goutieres syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.
