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Up to: Hereditary neuromuscular disease · Inherited neurodegenerative disorder · Motor neuron disorder

Hereditary motor neuron disease

An instance of motor neuron disease that is caused by an inherited modification of the individual's genome.

1 trial tagged with this condition →

  • Spinal muscular atrophy 107 trials · 117 incl. sub-types Sub-types →
  • Familial amyotrophic lateral sclerosis 2 trials · 29 incl. sub-types Sub-types →
  • Lateral sclerosis 24 trials Sub-types →
  • Riboflavin transporter deficiency 1 trial · 6 incl. sub-types Sub-types →
  • Distal hereditary motor neuropathy 0 trials · 4 incl. sub-types Sub-types →
  • ALS2-related motor neuron disease 0 trials Sub-types →
  • 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 Sub-types →

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