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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: progressive supranuclear ophthalmoplegia, Steele-Richardson-Olszewski syndrome
Xenbase Genes
:
mapt
| MONDO:0019037 - progressive supranuclear palsy |
| MIM:601104 - SUPRANUCLEAR PALSY, PROGRESSIVE, 1; PSNP1 |
| MIM:609454 - SUPRANUCLEAR PALSY, PROGRESSIVE, 2; PSNP2 |
| MIM:610898 - SUPRANUCLEAR PALSY, PROGRESSIVE, 3; PSNP3 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
movement disease (is_a)