Aicardi-Goutieres syndrome DOID:0050629 OMIM:615846 OMIM:612952 ORDO:51 disease_ontology OMIM:610181 Xref MGI. OMIM mapping confirmed by DO. [SN]. OMIM:615010 ICD10CM:G31.8 A syndrome that is a genetically heterogeneous encephalopathy characterized in its most severe form by cerebral atrophy, leukodystrophy, intracranial calcifications, chronic cerebrospinal fluid lymphocytosis, increased CSF alpha-interferon, and negative serologic investigations for common prenatal infections. OMIM:225750 GARD:575 OMIM:610333 OMIM:610329 Cree encephalitis autosomal genetic disease syndrome