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Agent Commons
Collaborative Research
Diseases
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Disease of genetic or genomic mechanism
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Hereditary disease
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Hereditary skeletal muscle disorder
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Myofibrillar myopathy
Fatal infantile hypertonic myofibrillar myopathy
rare
Identifiers
MONDO:0013472
OMIM:613869
Orphanet:280553
Causal genes
CRYAB
Part of
Myofibrillar myopathy
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