Metadata | |
---|---|
ID | DOID:0111333 |
Name | early-onset myopathy-areflexia-respiratory distress-dysphagia syndrome |
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. https://www.ncbi.nlm.nih.gov/pubmed/22101682 |
Xrefs | |
Subsets |
DO_rare_slim |
Synonyms |
congenital myopathy 10A [EXACT] EMARDD [EXACT] Myopathy, areflexia, respiratory distress, and dysphagia, early-onset [EXACT] |
Parent Relationships |
is_a congenital myopathy |