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Standards Ontologies Notations
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
Disease Ontology
DOID:480
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
MGI genotype (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
1813 DRD2 dopamine receptor D2
1949 EFNB3 ephrin B3
Displaying all 2 entries
Gene ID Gene Symbol Description Source
13489 Drd2 dopamine receptor D2
13643 Efnb3 ephrin B3
Displaying 1 entry
Gene ID Gene Symbol Description Source
24318 Drd2 dopamine receptor D2
Displaying 1 entry
Gene ID Gene Symbol Description Source
33007 Dop2R Dopamine 2-like receptor
Displaying 1 entry
Gene ID Gene Symbol Description Source Organism
378584 drd2.L dopamine receptor D2 L homeolog Xenopus laevis (African clawed frog)
Displaying 1 entry
Gene ID Gene Symbol Description Source
179347 dop-2 Dopamine receptor 2
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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