myofibrillar myopathy 10

Summary
Synonym
  • MFM10
Definition
A myofibrillar myopathy characterized by onset of muscle pain, cramping, and exercise fatigue in the first or second decades of life that has_material_basis_in homozygous or compound heterozygous mutation in the SVIL gene on chromosome 10p11.23.
Super Class
autosomal recessive disease myofibrillar myopathy
Disease Ontology
DOID:0112108
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6840 SVIL supervillin
Displaying 1 entry
Gene ID Gene Symbol Description Source
225115 Svil supervillin

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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