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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

Distal hereditary motor neuropathy type 2

rare

Identifiers: MONDO:0015352 Orphanet:139525
Part of: Neuronopathy, distal hereditary motor, autosomal dominant
Also known as: dHMN2 · distal spinal muscular atrophy type 2 · dSMA2

Subtypes

All diseases Rare only

Disease

Neuronopathy, distal hereditary motor, type 2A MONDO:0008025 HSPB8
Neuronopathy, distal hereditary motor, type 2B MONDO:0012080 HSPB1
Neuronopathy, distal hereditary motor, type 2C MONDO:0013243 HSPB3
Neuronopathy, distal hereditary motor, type 2D MONDO:0014259 FBXO38

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