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Amyoplasie congénitale
Anomalie congénitale
Anomalies multiples congénitales
Arthrogrypose
Arthrogrypose congénitale multiple
Arthrogryposis multiplex congénitale
Maladie ou lésion congénitale
Malformations congénitales multiples
Myodystrophie foetale
Raideur articulaire congénitale
SAI de l'encéphale

Translation of "Arthrogrypose congénitale multiple " (French → English) :

arthrogrypose congénitale multiple [ amyoplasie congénitale | arthrogryposis multiplex congénitale | raideur articulaire congénitale | arthrogrypose | myodystrophie foetale ]

arthrogryposis multiplex congenita [ amyoplasia congenita | myodystrophia fetalis | congenital multiple arthrogryposis ]
Os et articulations | Appareil locomoteur (Médecine) | Symptômes (Médecine)
Bones and Joints | Musculoskeletal System | Symptoms (Medicine)


Arthrogrypose congénitale multiple

Arthrogryposis multiplex congenita
WORLD HEALTH ORGANIZATION ICD-10: Q74.3
WORLD HEALTH ORGANIZATION ICD-10: Q74.3


Malformations congénitales multiples

Multiple congenital malformations
WORLD HEALTH ORGANIZATION ICD-10: Q89.7
WORLD HEALTH ORGANIZATION ICD-10: Q89.7


syndrome d'arthrogrypose multiple congénitale-face de siffleur

Illum syndrome
SNOMEDCT-BE (disorder) / 720514008
SNOMEDCT-BE (disorder) / 720514008


arthrogrypose multiple congénitale myogénique autosomique récessive

Autosomal recessive myogenic arthrogryposis multiplex congenita
SNOMEDCT-BE (disorder) / 764812008
SNOMEDCT-BE (disorder) / 764812008


Anomalie congénitale | Anomalies multiples congénitales | Maladie ou lésion congénitale | SAI de l'encéphale

Congenital:anomaly | deformity | disease or lesion | multiple anomalies | NOS of brain
WORLD HEALTH ORGANIZATION ICD-10: Q04.9
WORLD HEALTH ORGANIZATION ICD-10: Q04.9




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Arthrogrypose congénitale multiple

Date index:2024-02-22 -

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