dystonia 9

Summary
Definition
A dystonia that is characterized by paroxysmal choreoathetosis and progressive spastic paraplegia, with episodes often precipitated by alcohol, fatigue, or emotional stress, and that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the solute carrier family 2 member 1 (SLC2A1) gene on chromosome 1p34.
Super Class
autosomal dominant disease dystonia
External Links
Disease Ontology
DOID:0090044
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6513 SLC2A1 solute carrier family 2 member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
20525 Slc2a1 solute carrier family 2 (facilitated glucose transporter), member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
24778 Slc2a1 solute carrier family 2 member 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
38109 Glut1 Glucose transporter 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
852543 VVS1 Vvs1p

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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