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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
External Links
Disease Ontology
DOID:678
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
ORDO
OMIM
GARD
Related Genes
Displaying entries 11 - 14 of 14 in total
Gene ID Gene Symbol Description Source
5728 PTEN phosphatase and tensin homolog
7167 TPI1 triosephosphate isomerase 1
10724 OGA O-GlcNAcase
23583 SMUG1 single-strand-selective monofunctional uracil-DNA glycosylase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
18294 Ogg1 8-oxoguanine DNA-glycosylase 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
81528 Ogg1 8-oxoguanine DNA glycosylase
Displaying 1 entry
Gene ID Gene Symbol Description Source
31806 Ogg1 8-oxoguanine DNA glycosylase
Displaying 1 entry
Gene ID Gene Symbol Description Source
854942 OGG1 8-oxoguanine glycosylase OGG1
Related Glycoprotein
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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: August 19, 2024