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AMYOTROPHIE SPINALE [5 records]

Record 1 2025-04-30

English

Subject field(s)
  • Human Diseases - Various
  • Nervous System
  • Genetics
CONT

Spinal muscular atrophy (SMA) refers to a group of hereditary diseases that affect lower motor neurons.

OBS

SMA is classified into four main types, each varying in age of onset, severity, and approach to treatment.

French

Domaine(s)
  • Maladies humaines diverses
  • Système nerveux
  • Génétique
CONT

Le terme d'amyotrophie spinale est le nom donné à un groupe de maladies héréditaires caractérisées par la faiblesse et l'atrophie des muscles. Elle s'attaque aux cellules nerveuses (appelées neurones moteurs ou motoneurones) qui stimulent et commandent les muscles volontaires et entraîne leur destruction.

Spanish

Save record 1

Record 2 2025-03-25

English

Subject field(s)
  • Human Diseases
  • Nervous System
  • Muscles and Tendons
Universal entry(ies)
G12
classification system code, see observation
OBS

G12: code used in the International Statistical Classification of Diseases and Related Health Problems.

French

Domaine(s)
  • Maladies humaines
  • Système nerveux
  • Muscles et tendons
Entrée(s) universelle(s)
G12
classification system code, see observation
OBS

G12 : code de la Classification statistique internationale des maladies et des problèmes de santé connexes.

Spanish

Campo(s) temático(s)
  • Enfermedades humanas
  • Sistema nervioso
  • Músculos y tendones
Entrada(s) universal(es)
G12
classification system code, see observation
OBS

G12: código de la Clasificación Estadística Internacional de Enfermedades y Problemas Relacionados con la Salud.

Save record 2

Record 3 2025-03-25

English

Subject field(s)
  • Human Diseases
  • Nervous System
  • Muscles and Tendons
Universal entry(ies)
G12.9
classification system code, see observation
OBS

G12.9: code used in the International Statistical Classification of Diseases and Related Health Problems.

French

Domaine(s)
  • Maladies humaines
  • Système nerveux
  • Muscles et tendons
Entrée(s) universelle(s)
G12.9
classification system code, see observation
OBS

G12.9 : code de la Classification statistique internationale des maladies et des problèmes de santé connexes.

Spanish

Campo(s) temático(s)
  • Enfermedades humanas
  • Sistema nervioso
  • Músculos y tendones
Entrada(s) universal(es)
G12.9
classification system code, see observation
OBS

G12.9: código de la Clasificación Estadística Internacional de Enfermedades y Problemas Relacionados con la Salud.

Save record 3

Record 4 2024-09-23

English

Subject field(s)
  • Names of Special Years, Weeks, Days
  • Human Diseases
  • Nervous System
  • Muscles and Tendons
OBS

SMA Awareness Month strives to raise awareness of the condition caused by the deficiency of a motor neuron protein called SMN [survival motor neuron] and other rare forms of SMA that stem from chromosome mutations.

OBS

Spinal Muscular Atrophy Awareness Month takes place every year in August.

French

Domaine(s)
  • Désignations d'années, de semaines et de jours spéciaux
  • Maladies humaines
  • Système nerveux
  • Muscles et tendons
OBS

Le mois de sensibilisation à l'amyotrophie spinale a lieu chaque année au mois d'août.

Spanish

Save record 4

Record 5 2023-12-12

English

Subject field(s)
  • Human Diseases
  • Nervous System
  • Muscles and Tendons
Universal entry(ies)
G12.0
classification system code, see observation
OBS

G12.0: code used in the International Statistical Classification of Diseases and Related Health Problems.

French

Domaine(s)
  • Maladies humaines
  • Système nerveux
  • Muscles et tendons
Entrée(s) universelle(s)
G12.0
classification system code, see observation
OBS

G12.0 : code de la Classification statistique internationale des maladies et des problèmes de santé connexes.

Spanish

Campo(s) temático(s)
  • Enfermedades humanas
  • Sistema nervioso
  • Músculos y tendones
Entrada(s) universal(es)
G12.0
classification system code, see observation
CONT

Las atrofias musculares espinales de la infancia son enfermedades neuromusculares hereditarias, autosómicas, recesivas, caracterizadas por la degeneración de las neuronas motoras del asta anterior de la médula espinal. La atrofia muscular espinal tipo I (enfermedad de Werdnig-Hoffmann) es la forma más severa.

OBS

G12.0: código de la Clasificación Estadística Internacional de Enfermedades y Problemas Relacionados con la Salud.

Save record 5

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