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Diseases / Disease of genetic or genomic mechanism/ Hereditary disease/ Autosomal genetic disease/ Autosomal dominant disease/ Neuronopathy, distal hereditary motor, autosomal dominant

Neuronopathy, distal hereditary motor, autosomal dominant 10

rare

Identifiers: MONDO:0859300 OMIM:620080
Causal genes: EMILIN1
Part of: Neuronopathy, distal hereditary motor, autosomal dominant
Also known as: neuronopathy, distal hereditary motor, type X

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