|
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)