early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome

Summary
Synonym
  • EMARDD
  • Myopathy, areflexia, respiratory distress, and dysphagia, early-onset
  • congenital myopathy 10A
Definition
A congenital myopathy characterized by proximal and generalized muscle weakness, respiratory difficulties, joint contractures, and scoliosis that has_material_basis_in homozygous or compound heterozygous mutation in MEGF10 on chromosome 5q23.2.
Super Class
autosomal recessive disease congenital myopathy
External Links
Disease Ontology
DOID:0111333
Mondo Disease Ontology
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
84466 MEGF10 multiple EGF like domains 10
Displaying 1 entry
Gene ID Gene Symbol Description Source
70417 Megf10 multiple EGF-like-domains 10
Displaying 1 entry
Gene ID Gene Symbol Description Source
38218 drpr draper
Displaying 1 entry
Gene ID Gene Symbol Description Source
173064 ced-1 Cell death abnormality protein 1

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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