Becker muscular dystrophy

Summary
Synonym
  • Benign pseudohypertrophic muscular dystrophy
  • benign congenital myopathy
Definition
A muscular dystrophy that involves slowly worsening muscle weakness of the legs and pelvis, and has_material_basis_in X-linked recessive inheritance of mutation in the dystrophin gene on chromosome Xp21.
Super Class
muscular dystrophy
External Links
Disease Ontology
DOID:9883
Mondo Disease Ontology
UMLS
ORDO
OMIM
GARD
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 12 of 12 in total
Gene ID Gene Symbol Description Source
26033 ATRNL1 attractin like 1
79147 FKRP fukutin related protein
Related Glycoprotein
Displaying entry 11 - 11 of 11 in total
UniProt ID Protein Name Source
Q9H9S5 Ribitol 5-phosphate transferase FKRP

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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