autosomal recessive limb-girdle muscular dystrophy type 2H

Summary
Synonym
  • LGMD2H
  • limb-girdle muscular dystrophy due to TRIM32 deficiency
  • muscular dystrophy Hutterite type
  • sarcotubular myopathy
Definition
An autosomal recessive limb-girdle muscular dystrophy that has_material_basis_in mutation in the gene encoding tripartite motif-containing protein-32 (TRIM32) on chromosome 9q.
Super Class
autosomal recessive limb-girdle muscular dystrophy
Disease Ontology
DOID:0110282
Mondo Disease Ontology
ORDO
OMIM
MGI genotype (from TogoID)

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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