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Distal hereditary motor neuropathy

MONDO:0018894

Also known as: dHMN, dSMA, distal spinal muscular atrophy, neuronopathy, distal hereditary motor

31 clinical trials for this condition and its sub-types.

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Sub-types

Neuronopathy, distal hereditary motor, autosomal recessive 8 (2) Autosomal recessive distal spinal muscular atrophy 1 (1) Autosomal recessive distal spinal muscular atrophy 2 (0) COQ7-related distal hereditary motor neuropathy (0) Distal hereditary motor neuropathy type 2 (0) Distal hereditary motor neuropathy type 7 (0) Early-onset progressive encephalopathy-spastic ataxia-distal spinal muscular atrophy syndrome (0) Hereditary spastic paraplegia 17 (0) Myopathy, myofibrillar, 13, with rimmed vacuoles (0) Neuronopathy, distal hereditary motor, autosomal dominant (0) Neuronopathy, distal hereditary motor, autosomal dominant 1 (0) Neuronopathy, distal hereditary motor, autosomal dominant 10 (0) Neuronopathy, distal hereditary motor, autosomal dominant 11 (0) Neuronopathy, distal hereditary motor, autosomal dominant 15 (0) Neuronopathy, distal hereditary motor, autosomal dominant 8 (0) Neuronopathy, distal hereditary motor, autosomal recessive (0) Neuronopathy, distal hereditary motor, autosomal recessive 10 (0) Neuronopathy, distal hereditary motor, autosomal recessive 11, with spasticity (0) Neuronopathy, distal hereditary motor, autosomal recessive 3 (0) Neuronopathy, distal hereditary motor, autosomal recessive 4 (0)

Broader categories

Disease (618) Nervous system disorder (217) Hereditary disease (172) Neurodegenerative disease (155) Peripheral nervous system disorder (107) Neuromuscular disease (98) Central nervous system disorder (97) Peripheral neuropathy (90) Motor neuron disorder (59) Human disease (14)
Trials to join now! 17 Not yet recruiting 2 Not yet finished but already full! 5 Completed 7
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