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Standards Ontologies Notations
progressive supranuclear palsy

Summary
Synonym
  • Steele-Richardson-Olszewski syndrome
  • progressive supranuclear ophthalmoplegia
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.
Super Class
movement disease
Disease Ontology
DOID:678
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
Related Genes
Displaying all 5 entries
Gene ID Gene Symbol Description Source
4137 MAPT microtubule associated protein tau
4968 OGG1 8-oxoguanine DNA glycosylase
5608 MAP2K6 mitogen-activated protein kinase kinase 6
6647 SOD1 superoxide dismutase 1
23435 TARDBP TAR DNA binding protein
Displaying all 3 entries
Gene ID Gene Symbol Description Source
17762 Mapt microtubule-associated protein tau
18294 Ogg1 8-oxoguanine DNA-glycosylase 1
20655 Sod1 superoxide dismutase 1, soluble
Displaying 1 entry
Gene ID Gene Symbol Description Source
81528 Ogg1 8-oxoguanine DNA glycosylase
Displaying all 2 entries
Gene ID Gene Symbol Description Source
31806 Ogg1 8-oxoguanine DNA glycosylase
36232 Sod3 Superoxide dismutase 3
Displaying all 2 entries
Gene ID Gene Symbol Description Source
853313 PBS2 mitogen-activated protein kinase kinase PBS2
854942 OGG1 8-oxoguanine glycosylase OGG1
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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: December 9, 2024