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 11 - 20 of 26 in total
HPO ID HPO Term
HP:0100299 Muscle fiber inclusion bodies
HP:0003691 Scapular winging
HP:0008180 Mildly elevated creatine kinase
HP:0000821 Hypothyroidism
HP:0003724 Shoulder girdle muscle atrophy
HP:0008963 Tibialis muscle weakness
HP:0001436 Abnormality of the foot musculature
HP:0012515 Hip flexor weakness
HP:0003458 EMG: myopathic abnormalities
HP:0006467 Limited shoulder movement
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