Ullrich congenital muscular dystrophy

Summary
Synonym
  • ULLRICH DISEASE
  • Ullrich scleroatonic muscular dystrophy
Definition
A congenital muscular dystrophy that is characterized by muscle weakness and respiratory depression and has_material_basis_in mutation in the COL6A1, COL6A2 and COL6A3 that produce components of type VI collagen.
Super Class
autosomal dominant disease autosomal recessive disease congenital muscular dystrophy
External Links
Disease Ontology
DOID:0050558
Mondo Disease Ontology
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying all 2 entries
Gene ID Gene Symbol Description Source
1291 COL6A1 collagen type VI alpha 1 chain
1464 CSPG4 chondroitin sulfate proteoglycan 4
Displaying 1 entry
Gene ID Gene Symbol Description Source
12833 Col6a1 collagen, type VI, alpha 1
Related Glycoprotein
Displaying 1 entry
UniProt ID Protein Name Source
Q6UVK1 Chondroitin sulfate proteoglycan 4

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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