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Amyoplasia congenita
Arthrochalasis-multiplex congenita
Arthrogryposis multiplex congenita
Congenital multiple arthrogryposis
Cutis hyperelastica
EDS
Ehlers-Danlos syndrome
Guerin-Stern syndrome
Myodystrophia fetalis

Translation of "Arthrogryposis multiplex congenita " (English → French) :

arthrogryposis multiplex congenita [ amyoplasia congenita | myodystrophia fetalis | congenital multiple arthrogryposis ]

arthrogrypose congénitale multiple [ amyoplasie congénitale | arthrogryposis multiplex congénitale | raideur articulaire congénitale | arthrogrypose | myodystrophie foetale ]
Bones and Joints | Musculoskeletal System | Symptoms (Medicine)
Os et articulations | Appareil locomoteur (Médecine) | Symptômes (Médecine)


arthrogryposis multiplex congenita | Guerin-Stern syndrome

arthrogrypose
IATE - Health
IATE - Health


Arthrogryposis multiplex congenita

Arthrogrypose congénitale multiple
WORLD HEALTH ORGANIZATION ICD-10: Q74.3
WORLD HEALTH ORGANIZATION ICD-10: Q74.3


Autosomal recessive myogenic arthrogryposis multiplex congenita

arthrogrypose multiple congénitale myogénique autosomique récessive
SNOMEDCT-BE (disorder) / 764812008
SNOMEDCT-BE (disorder) / 764812008


SYNE1 (spectrin repeat containing nuclear envelope protein 1) related arthrogryposis multiplex congenita

AMC myogénique autosomique récessive
SNOMEDCT-BE (disorder) / 764812008
SNOMEDCT-BE (disorder) / 764812008


arthrochalasis-multiplex congenita | cutis hyperelastica | Ehlers-Danlos syndrome | EDS [Abbr.]

dermatosparaxie | maladie d'Ehler-Danlos
IATE - Health
IATE - Health




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'Arthrogryposis multiplex congenita'

Date index:2021-06-14 -

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