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AttributesValues
type
sameAs
notation
  • C10.228.854.139
  • C10.574.562.250
  • C10.574.950.050
  • C10.668.467.250
  • C18.452.845.800.050
alternative label
  • Maladie de Charcot
  • Amyotrophic Lateral Sclerosis, Parkinsonism-Dementia Complex of Guam
  • Disease, Lou-Gehrigs
  • Lou Gehrig Disease
  • Maladie de Guam
  • Maladie de Lou Gehrig
  • Maladie de l'ile de Guam
  • Sclerosis, Amyotrophic Lateral
  • Syndrome de Guam
  • Amyotrophic Lateral Sclerosis Parkinsonism Dementia Complex 1
  • Sclérose latérale amyotrophique de l'île de Guam
  • Amyotrophic Lateral Sclerosis
  • Charcot Disease
  • Gehrig Disease
  • Gehrig's Disease
  • Guam Disease
  • Lou Gehrig's Disease
  • Association de sclérose latérale amyotrophique, de maladie de Parkinson et de démence de l'ile de Guam
  • Motor Neuron Disease, Amyotrophic Lateral Sclerosis
  • Association de sclérose latérale amyotrophique, de maladie de Parkinson et de démence de type 1
  • Amyotrophic Lateral Sclerosis With Dementia
  • Amyotrophic Lateral Sclerosis, Guam Form
  • Dementia With Amyotrophic Lateral Sclerosis
  • Disease, Guam
  • Démence avec sclérose latérale amyotrophique
  • Guam Form of Amyotrophic Lateral Sclerosis
  • SLA (Sclérose Latérale Amyotrophique)
  • Sclérose latérale amyotrophique avec démence
  • Amyotrophic Lateral Sclerosis-Parkinsonism-Dementia Complex 1
  • Gehrigs Disease
  • Lou-Gehrigs Disease
  • Maladie de Gehrig
  • Sclérose latérale amyotrophique de l'ile de Guam
  • Syndrome de l'ile de Guam
  • Amyotrophic Lateral Sclerosis, Parkinsonism Dementia Complex of Guam
  • ALS - Amyotrophic Lateral Sclerosis
  • ALS Amyotrophic Lateral Sclerosis
preferred label
  • Sclérose latérale amyotrophique
is in scheme
note
  • A degenerative disorder affecting upper MOTOR NEURONS in the brain and lower motor neurons in the brain stem and SPINAL CORD. Disease onset is usually after the age of 50 and the process is usually fatal within 3 to 6 years. Clinical manifestations include progressive weakness, atrophy, FASCICULATION, hyperreflexia, DYSARTHRIA, dysphagia, and eventual paralysis of respiratory function. Pathologic features include the replacement of motor neurons with fibrous ASTROCYTES and atrophy of anterior SPINAL NERVE ROOTS and corticospinal tracts. (From Adams et al., Principles of Neurology, 6th ed, pp1089-94)
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