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Metadata
ID	DOID:0050629
Name	Aicardi-Goutieres syndrome
Definition	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. http://omim.org/entry/225750, http://www.ncbi.nlm.nih.gov/books/NBK1475/
Xrefs	GARD:575 ICD10CM:G31.8 OMIM:225750 OMIM:610181 OMIM:610329 OMIM:610333 OMIM:612952 OMIM:615010 OMIM:615846 OMIM:PS225750 ORDO:51
Subsets	DO_rare_slim
Synonyms	AGS [EXACT] Cree encephalitis [EXACT]
Parent Relationships	is_a syndrome is_a autosomal genetic disease