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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

GARD:12199

OMIM:614399

ORDO:439212

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

is_a autosomal recessive disease

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