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Summary Literature (0)
DOID:1442 - Alpers syndrome

Disease Ontology Definition:A cerebral degeneration that results in progressive degeneration of grey matter in the cerebrum and has_symptom convulsions.

Synonyms: ALPERS PROGRESSIVE INFANTILE POLIODYSTROPHY, ALPERS-HUTTENLOCHER SYNDROME, Alper's syndrome, Alpers' disease or gray-matter degeneration, MITOCHONDRIAL DNA DEPLETION SYNDROME 4A, progressive sclerosing poliodystrophy

Echinobase Genes :

OMIM:203700 - mitochondrial dna depletion syndrome 4a (alpers type); mtdps4a

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): cerebral degeneration (is_a)