Hereditary motor neuron disease

Part of

Sub-types of Hereditary motor neuron disease

• Spinal muscular atrophy 107 trials · 117 incl. sub-types
  19 sub-types

  • Proximal spinal muscular atrophy 14 trials · 42 incl. sub-types Sub-types →
  • Autosomal recessive distal spinal muscular atrophy 1 2 trials
  • Bulbospinal muscular atrophy 1 trial Sub-types →
  • X-linked distal spinal muscular atrophy type 3 0 trials
  • Adult-onset proximal spinal muscular atrophy, autosomal dominant 0 trials
  • Autosomal recessive distal spinal muscular atrophy 2 0 trials
  • Infantile-onset X-linked spinal muscular atrophy 0 trials
  • Neuronopathy, distal hereditary motor, autosomal dominant 0 trials Sub-types →
  • Neuronopathy, distal hereditary motor, autosomal recessive 3 0 trials
  • Neuronopathy, distal hereditary motor, autosomal recessive 4 0 trials
  • Neuronopathy, distal hereditary motor, autosomal recessive 5 0 trials
  • Scapuloperoneal spinal muscular atrophy, autosomal dominant 0 trials
  • Scapuloperoneal spinal muscular atrophy, autosomal recessive 0 trials
  • Spinal muscular atrophy type 0 0 trials
  • Spinal muscular atrophy with respiratory distress type 2 0 trials
  • Spinal muscular atrophy, Ryukyuan type 0 trials
  • Spinal muscular atrophy, facioscapulohumeral type 0 trials
  • Spinal muscular atrophy, segmental 0 trials
  • Spinal muscular atrophy-progressive myoclonic epilepsy syndrome 0 trials
• Familial amyotrophic lateral sclerosis 2 trials · 29 incl. sub-types
  30 sub-types

  • Spinocerebellar ataxia type 2 10 trials Sub-types →
  • Amyotrophic lateral sclerosis type 1 8 trials
  • Frontotemporal dementia and/or amyotrophic lateral sclerosis 1 5 trials
  • Amyotrophic lateral sclerosis type 10 3 trials
  • Amyotrophic lateral sclerosis type 4 1 trial
  • Amyotrophic lateral sclerosis type 6 1 trial
  • Amyotrophic lateral sclerosis type 7 1 trial
  • Amyotrophic lateral sclerosis 26 with or without frontotemporal dementia 0 trials
  • Amyotrophic lateral sclerosis 27, juvenile 0 trials
  • Amyotrophic lateral sclerosis 28 0 trials
  • Amyotrophic lateral sclerosis type 11 0 trials
  • Amyotrophic lateral sclerosis type 12 0 trials
  • Amyotrophic lateral sclerosis type 15 0 trials
  • Amyotrophic lateral sclerosis type 18 0 trials
  • Amyotrophic lateral sclerosis type 19 0 trials
  • Amyotrophic lateral sclerosis type 20 0 trials
  • Amyotrophic lateral sclerosis type 21 0 trials
  • Amyotrophic lateral sclerosis type 22 0 trials
  • Amyotrophic lateral sclerosis type 23 0 trials
  • Amyotrophic lateral sclerosis type 3 0 trials
  • Amyotrophic lateral sclerosis type 8 0 trials
  • Amyotrophic lateral sclerosis type 9 0 trials
  • Frontotemporal dementia and/or amyotrophic lateral sclerosis 2 0 trials
  • Frontotemporal dementia and/or amyotrophic lateral sclerosis 3 0 trials
  • Frontotemporal dementia and/or amyotrophic lateral sclerosis 4 0 trials
  • Frontotemporal dementia and/or amyotrophic lateral sclerosis 5 0 trials
  • Frontotemporal dementia and/or amyotrophic lateral sclerosis 6 0 trials
  • Frontotemporal dementia and/or amyotrophic lateral sclerosis 7 0 trials
  • Frontotemporal dementia and/or amyotrophic lateral sclerosis 8 0 trials
  • Juvenile amyotrophic lateral sclerosis 0 trials Sub-types →
• Lateral sclerosis 24 trials
  2 sub-types

  • Primary lateral sclerosis, adult, 1 1 trial
  • Juvenile primary lateral sclerosis 0 trials
• Riboflavin transporter deficiency 1 trial · 6 incl. sub-types
  3 sub-types

  • Progressive bulbar palsy 5 trials Sub-types →
  • Brown-Vialetto-van Laere syndrome 1 0 trials
  • Brown-Vialetto-van Laere syndrome 2 0 trials
• Distal hereditary motor neuropathy 0 trials · 4 incl. sub-types
  3 sub-types

  • Neuronopathy, distal hereditary motor, autosomal recessive 0 trials · 4 incl. sub-types Sub-types →
  • X-linked distal spinal muscular atrophy type 3 0 trials
  • Neuronopathy, distal hereditary motor, autosomal dominant 0 trials Sub-types →
• ALS2-related motor neuron disease 0 trials
  3 sub-types

  • Amyotrophic lateral sclerosis type 2, juvenile 0 trials
  • Infantile-onset ascending hereditary spastic paralysis 0 trials
  • Juvenile primary lateral sclerosis 0 trials
• Motor neuron disease with dementia and ophthalmoplegia 0 trials
• Neurogenic scapuloperoneal syndrome, Kaeser type 0 trials
• Prenatal-onset spinal muscular atrophy with congenital bone fractures 0 trials
  2 sub-types

  • Spinal muscular atrophy with congenital bone fractures 1 0 trials
  • Spinal muscular atrophy with congenital bone fractures 2 0 trials