syndromic intellectual disability inborn error of immunity autosomal recessive disease obsolete Moyamoya syndrome Aicardi-Goutieres syndrome https://github.com/monarch-initiative/mondo/issues/6878 https://github.com/monarch-initiative/mondo/issues/7365 https://www.malacards.org/card/aicardi_goutieres_syndrome encephalopathy, familial infantile, with calcification of basal ganglia and chronic cerebrospinal fluid lymphocytosis MONDO:0018866 encephalopathy with intracranial calcification and chronic lymphocytosis of cerebrospinal fluid ICD9:333.0 NORD:111728 pseudotoxoplasmosis syndrome AGS NANDO:2100244 SCTID:230312006 UMLS:C0393591 DOID:0050629 NANDO:1200996 Aicardi-Goutières Syndrome NANDO:2200893 MESH:C535607 encephalopathy with basal ganglia calcification GARD:0000575 Aicardi-Goutieres syndrome (AGS) is an inherited, subacute encephalopathy characterized by the association of basal ganglia calcification, leukodystrophy and cerebrospinal fluid (CSF) lymphocytosis. Aicardi Goutieres syndrome Orphanet:51 MEDGEN:97953 Cree encephalitis OMIMPS:225750 leukodystrophy hereditary disorder of connective tissue type 1 interferonopathy of childhood