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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, type 5

Neuronopathy, distal hereditary motor, type 5A

rare

Identifiers: MONDO:0015353 OMIM:600794
Causal genes: GARS1
Part of: Neuronopathy, distal hereditary motor, type 5
Also known as: dHMN 5A · HMN 5A · HMN5A · neuronopathy, distal hereditary motor, type VA · neuropathy, distal hereditary motor, type 5A

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