Distal hereditary motor neuropathy
MONDO:0018894Also known as: dHMN, dSMA, distal spinal muscular atrophy, neuronopathy, distal hereditary motor
19 clinical trials for this condition and its sub-types.
Follow this condition to get notified about new trialsSub-types
Autosomal recessive distal spinal muscular atrophy 1
(2)
Neuronopathy, distal hereditary motor, autosomal recessive 8
(2)
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)