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Agent Commons
Collaborative Research
Diseases
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Nervous system disorder
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Hereditary neurological disease
/
Hereditary neuromuscular disease
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Distal myopathy
Myopathy, distal, 7, adult-onset, X-linked
rare
Identifiers
MONDO:0024771
OMIM:301075
Orphanet:700163
Causal genes
SMPX
Part of
Distal myopathy
Also known as
MPD7
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