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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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Autosomal genetic disease
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Autosomal recessive disease
Scapuloperoneal spinal muscular atrophy, autosomal recessive
rare
Identifiers
MONDO:0010058
OMIM:271220
Part of
Autosomal recessive disease
Spinal muscular atrophy
Also known as
spinal muscular atrophy, scapuloperoneal
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