Bethlem myopathy

Summary
Synonym
  • benign congenital muscular dystrophy
Definition
A congenital muscular dystrophy that is characterized by myopathy and joint contractures that progresses slowly, has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the COL6A1 gene, the COL6A2 gene, or the COL6A3 gene.
Super Class
congenital muscular dystrophy
Disease Ontology
DOID:0050663
Mondo Disease Ontology
MeSH
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying all 4 entries
Gene ID Gene Symbol Description Source
1291 COL6A1 collagen type VI alpha 1 chain
1292 COL6A2 collagen type VI alpha 2 chain
1293 COL6A3 collagen type VI alpha 3 chain
1303 COL12A1 collagen type XII alpha 1 chain
Displaying all 4 entries
Gene ID Gene Symbol Description Source
12816 Col12a1 collagen, type XII, alpha 1
12833 Col6a1 collagen, type VI, alpha 1
12834 Col6a2 collagen, type VI, alpha 2
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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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