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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 dominant disease
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Neuronopathy, distal hereditary motor, autosomal dominant
Neuronopathy, distal hereditary motor, autosomal dominant 11
rare
Identifiers
MONDO:0957875
OMIM:620528
Causal genes
SPTAN1
Part of
Neuronopathy, distal hereditary motor, autosomal dominant
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