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Summary Literature (0)
DOID:4252 - Alexander disease

Disease Ontology Definition:A leukodystrophy that is characterized by the destruction of white matter and the formation of Rosenthal fibers consisting of abnormal clumps of protein that accumulate in astrocytes.

Synonyms: Alexander's disease

Xenbase Genes : ndufv1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008752 - Alexander disease

MIM:
MIM:203450 - ALEXANDER DISEASE; ALXDRD

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view
Parent(s): autosomal dominant disease (is_a), leukodystrophy (is_a)