episodic kinesigenic dyskinesia 1

Summary
Synonym
  • Paroxysmal kinesigenic choreoathetosis
Definition
A dystonia characterized by recurrent brief involuntary hyperkinesias triggered by sudden movements that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the proline-rich transmembrane protein 2 gene (PRRT2) on chromosome 16p11.
Super Class
autosomal dominant disease dystonia
External Links
Disease Ontology
DOID:0090053
Mondo Disease Ontology
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 18 of 18 in total
Gene ID Gene Symbol Description Source
5313 PKLR pyruvate kinase L/R
5728 PTEN phosphatase and tensin homolog
6401 SELE selectin E
8394 PIP5K1A phosphatidylinositol-4-phosphate 5-kinase type 1 alpha
9514 GAL3ST1 galactose-3-O-sulfotransferase 1
10559 SLC35A1 solute carrier family 35 member A1
56623 INPP5E inositol polyphosphate-5-phosphatase E
342372 PKD1L3 polycystin 1 like 3, transient receptor potential channel interacting

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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