movement disease

Summary
Definition
A brain disease that is characterized by a clinical syndrome of either hyperkinetic movement or hyperkinetic movement unrelated to weakness or spasticity.
Super Class
brain disease
External Links
Disease Ontology
DOID:480
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
MGI genotype (from TogoID)
Related Genes
Displaying entries 21 - 30 of 33 in total
Gene ID Gene Symbol Description Source
5538 PPT1 palmitoyl-protein thioesterase 1
5621 PRNP prion protein (Kanno blood group)
5660 PSAP prosaposin
5728 PTEN phosphatase and tensin homolog
6448 SGSH N-sulfoglucosamine sulfohydrolase
6515 SLC2A3 solute carrier family 2 member 3
7915 ALDH5A1 aldehyde dehydrogenase 5 family member A1
8803 SUCLA2 succinate-CoA ligase ADP-forming subunit beta
22854 NTNG1 netrin G1
23556 PIGN phosphatidylinositol glycan anchor biosynthesis class N

About Release Notes Help Feedback

Click here to visit the beta site.


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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024