dystonia 27

Summary
Definition
A segmental dystonia characterized by autosomal recessive inheritance of segmental isolated dystonia mainly affecting the craniocervical region and upper limbs with onset in the first 2 decades of life that has_material_basis_in autosomal recessive inheritance of compound heterozygous mutation in the collagen type VI alpha-3 gene on chromosome 2q37.
Super Class
autosomal recessive disease segmental dystonia
Disease Ontology
DOID:0090050
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
1293 COL6A3 collagen type VI alpha 3 chain
Displaying 1 entry
Gene ID Gene Symbol Description Source
12835 Col6a3 collagen, type VI, alpha 3
Displaying 1 entry
Gene ID Gene Symbol Description Source
182256 R193.2 VWFA domain-containing protein

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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