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Metadata
ID	DOID:0081355
Name	congenital myopathy 22B
Definition	A congenital myopathy that is characterized by in utero onset of severe muscle weakness manifest as fetal akinesia and that has_material_basis_in homozygous or compound heterozygous mutation in the SCN4A gene on chromosome 17q23. https://pubmed.ncbi.nlm.nih.gov/26700687/
Xrefs	MIM:620369
Parent Relationships	is_a congenital myopathy is_a autosomal recessive disease
Subclass Logical Relationships	has material basis in some autosomal recessive inheritance