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Disease Ontology Browser
Alpers syndrome (DOID:1442)
Synonyms: Alper's syndrome; ALPERS PROGRESSIVE INFANTILE POLIODYSTROPHY; Alpers' disease or gray-matter degeneration; ALPERS-HUTTENLOCHER SYNDROME; MITOCHONDRIAL DNA DEPLETION SYNDROME 4A; progressive sclerosing poliodystrophy
Alt IDs: OMIM:203700, ICD10CM:G31.81, MESH:D002549, NCI:C35257, UMLS_CUI:C0205710
Definition: A cerebral degeneration that results in progressive degeneration of grey matter in the cerebrum and has_symptom convulsions.


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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
06/20/2017
MGI 6.10
The Jackson Laboratory