distal myopathy with rimmed vacuoles

Summary
Definition
A distal myopathy that is characterized by adult onset of muscle weakness affecting the distal upper and lower limbs, which may result in walking difficulties, as well as proximal weakness of the shoulder girdle muscles and that has_material_basis_in by heterozygous mutation in the SQSTM1 gene on chromosome 5q35.
Super Class
autosomal dominant disease distal myopathy
External Links
Disease Ontology
DOID:0081363
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
8878 SQSTM1 sequestosome 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
18412 Sqstm1 sequestosome 1
The Human Phenotype Ontology
Displaying entries 1 - 10 of 26 in total
HPO ID HPO Term
HP:0007210 Lower limb amyotrophy
HP:0003547 Shoulder girdle muscle weakness
HP:0012548 Fatty replacement of skeletal muscle
HP:0001638 Cardiomyopathy
HP:0009027 Foot dorsiflexor weakness
HP:0003731 Quadriceps muscle weakness
HP:0001324 Muscle weakness
HP:0006251 Limited wrist extension
HP:0010628 Facial palsy
HP:0003438 Absent Achilles reflex
Displaying 1 entry
Gene ID Gene Symbol Description
10020 GNE glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase

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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