FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term autosomal recessive limb-girdle muscular dystrophy type 26 ID (Ontology) DOID:0061131 (Human Disease)
Definition An autosomal recessive limb-girdle muscular dystrophy characterized by adult-onset weakness that primarily affects the proximal muscles of the lower limbs that has_material_basis_in homozygous mutation in the POPDC3 gene on chromosome 6q21.
Also Known As "LGMDR26"
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 Genes
 autosomal recessive limb-girdle muscular dystrophy type 26       1
 for disease ribbon | autosomal recessive limb-girdle muscular dystrophy type 26       1
 model of | autosomal recessive limb-girdle muscular dystrophy type 26       1
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autosomal recessive disease_____
limb-girdle muscular dystrophy__|
                                autosomal recessive limb-girdle muscular dystrophy
                                 |__autosomal recessive limb-girdle muscular dystrophy type 26  1 rec.
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Is a autosomal recessive limb-girdle muscular dystrophy
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Synonyms
  • "LGMDR26" EXACT OMO:0003012
Secondary IDs
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MIM:618848