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Summary Literature (0)
DOID:678 - progressive supranuclear palsy


Disease Ontology Definition:A movement disease that is characterized by serious and progressive problems with control of gait and balance, along with complex eye movement and thinking problems. It involves gradual deterioration and death of specific volumes of the brain.

Synonyms: Steele-Richardson-Olszewski syndrome, progressive supranuclear ophthalmoplegia

Xenbase Genes : mapt

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0019037 - progressive supranuclear palsy

OMIM:
OMIM:601104 - SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1
OMIM:609454 - SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2
OMIM:610898 - SUPRANUCLEAR PALSY, PROGRESSIVE, 3; PSNP3

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

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