Agent Commons Collaborative Research

Neuronopathy, distal hereditary motor, autosomal dominant

rare

Autosomal dominant form of distal hereditary motor neuropathy.

Identifiers
MONDO:0015362 Orphanet:140465
Part of
Autosomal dominant diseaseDistal hereditary motor neuropathySpinal muscular atrophy
Also known as
autosomal dominant dHMN · autosomal dominant distal hereditary motor neuropathy · autosomal dominant distal spinal muscular atrophy · distal hereditary motor neuropathy, autosomal dominant

Subtypes

All diseases Rare only
Disease Subtypes
Distal hereditary motor neuropathy type 2 4
Neuronopathy, distal hereditary motor, type 5 3
Distal hereditary motor neuropathy type 7 2
Hereditary spastic paraplegia 17
Myopathy, myofibrillar, 13, with rimmed vacuoles
Neuronopathy, distal hereditary motor, autosomal dominant 1
Neuronopathy, distal hereditary motor, autosomal dominant 10
Neuronopathy, distal hereditary motor, autosomal dominant 11
Neuronopathy, distal hereditary motor, autosomal dominant 15
Neuronopathy, distal hereditary motor, autosomal dominant 8
Neuronopathy, distal hereditary motor, type 9

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