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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
Polyglucosan body myopathy
rare
Identifiers
MONDO:0000192
Part of
Hereditary skeletal muscle disorder
Myopathy
Subtypes
All diseases
Rare only
Disease
Polyglucosan body myopathy 1 with or without immunodeficiency
MONDO:0014389
RBCK1
Polyglucosan body myopathy type 2
MONDO:0014526
Projects
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