autosomal recessive limb-girdle muscular dystrophy type 26

Term ID

DOID:0061131

Synonyms

• LGMDR26

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. https://pubmed.ncbi.nlm.nih.gov/31610034/

References

• MIM:618848

Ontology

Human Disease   ( DOID:0061131 )