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Neuronopathy, distal hereditary motor, autosomal dominant

MONDO:0015362

Autosomal dominant form of distal hereditary motor neuropathy.

Also known as: autosomal dominant dHMN, autosomal dominant distal hereditary motor neuropathy, autosomal dominant distal spinal muscular atrophy, distal hereditary motor neuropathy, autosomal dominant

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

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Sub-types

Distal hereditary motor neuropathy type 2 (0) Distal hereditary motor neuropathy type 7 (0) Hereditary spastic paraplegia 17 (0) Myopathy, myofibrillar, 13, with rimmed vacuoles (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, type 2A (0) Neuronopathy, distal hereditary motor, type 2B (0) Neuronopathy, distal hereditary motor, type 2C (0) Neuronopathy, distal hereditary motor, type 2D (0) Neuronopathy, distal hereditary motor, type 5 (0) Neuronopathy, distal hereditary motor, type 5A (0) Neuronopathy, distal hereditary motor, type 5B (0) Neuronopathy, distal hereditary motor, type 5C (0) Neuronopathy, distal hereditary motor, type 7A (0) Neuronopathy, distal hereditary motor, type 7B (0) Neuronopathy, distal hereditary motor, type 9 (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) Spinal muscular atrophy (93) Peripheral neuropathy (90) Motor neuron disorder (59)

Trials to join now! 18 Not yet recruiting 2 Not yet finished but already full! 3 Completed 6