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Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
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Hereditary neuromuscular disease
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X-linked myopathy with excessive autophagy
Myopathy, autophagic vacuolar, infantile-onset
rare
Identifiers
MONDO:0012286
OMIM:609500
Part of
X-linked myopathy with excessive autophagy
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