About   Help   FAQ
Disease Ontology Browser
Aicardi-Goutieres syndrome (DOID:0050629)
Alliance: disease page
Synonyms: Cree encephalitis
Alt IDs: OMIM:225750, OMIM:610181, OMIM:610329, OMIM:610333, OMIM:612952, OMIM:615010, OMIM:615846, ICD10CM:G31.8, OMIM:PS225750, ORDO:51
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.

Disease References using Mouse Models (5)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
MGI 6.22
The Jackson Laboratory