dystonia

Summary
Synonym
  • dystonic disease
Definition
A movement disease that is characterized by involuntary muscle contractions causing repetitive or twisting movements.
Super Class
movement disease
External Links
Disease Ontology
DOID:543
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying entries 61 - 70 of 71 in total
Gene ID Gene Symbol Description Source
57462 MYORG myogenesis regulating glycosidase (putative)
64116 SLC39A8 solute carrier family 39 member 8
79143 MBOAT7 membrane bound O-acyltransferase domain containing 7
79944 L2HGDH L-2-hydroxyglutarate dehydrogenase
79947 DHDDS dehydrodolichyl diphosphate synthase subunit
80055 PGAP1 post-GPI attachment to proteins inositol deacylase 1
81562 LMAN2L lectin, mannose binding 2 like
113612 CYP2U1 cytochrome P450 family 2 subfamily U member 1
148789 B3GALNT2 beta-1,3-N-acetylgalactosaminyltransferase 2
197322 ACSF3 acyl-CoA synthetase family member 3

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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