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Metadata
ID	DOID:0080309
Name	fatal infantile hypertonic myofibrillar myopathy
Definition	A myofibrillar myopathy that has_material_basis_in homozygous mutation in the CRYAB gene on chromosome 11q23. https://www.ncbi.nlm.nih.gov/pubmed/23995273
Xrefs	MIM:613869
Parent Relationships	is_a myofibrillar myopathy is_a autosomal recessive disease