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Amyoplasia congenita
Arthrogryposis multiplex congenita
Congenital anomaly
Congenital multiple arthrogryposis
Deformity
Disease or lesion
Multiple anomalies
Multiple congenital exostoses
Myodystrophia fetalis
NOS of brain

Translation of "congenital multiple arthrogryposis " (English → French) :

arthrogryposis multiplex congenita [ amyoplasia congenita | myodystrophia fetalis | congenital multiple arthrogryposis ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
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)
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
Congenital multiple pituitary hormone deficiency including somatotroph, thyrotroph, lactotroph, corticotroph or gonadotroph deficiencies, due to mutations of pituitary transcription factors involved in pituitary ontogenesis. Rare when compared with t
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
déficits hypohysaires multiples de cause génétique identifée
SNOMEDCT-BE (disorder) / 718182008
SNOMEDCT-BE (disorder) / 718182008
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Belongs to the group of multiple congenital anomalies/mental retardation syndromes with intellectual deficit, distinctive facies (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart def
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome de McDonough
SNOMEDCT-BE (upward slanting palpebral fissures, squint), kyphoscoliosis, diastasis recti, cryptorchidism, and a congenital heart def / 715441004
SNOMEDCT-BE (disorder) / 715441004
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
A multiple congenital anomalies/dysmorphic syndrome with characteristics of multiple skeletal malformations (short femora and humeri, bilateral absence of metatarsal and metacarpal bone in hands and feet, bilateral partial syndactyly of fingers and t
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome de Verloove-Van Horick-Brubakk
SNOMEDCT-BE (short femora and humeri, bilateral absence of metatarsal and metacarpal bone in hands and feet, bilateral partial syndactyly of fingers and t / 764697003
SNOMEDCT-BE (disorder) / 764697003
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Congenital:anomaly | deformity | disease or lesion | multiple anomalies | NOS of brain
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Anomalie congénitale | Anomalies multiples congénitales | Maladie ou lésion congénitale | SAI de l'encéphale
WORLD HEALTH ORGANIZATION ICD-10: Q04.9
WORLD HEALTH ORGANIZATION ICD-10: Q04.9
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Multiple congenital exostoses
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Exostoses multiples congénitales
WORLD HEALTH ORGANIZATION ICD-10: Q78.6
WORLD HEALTH ORGANIZATION ICD-10: Q78.6
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Congenital malformation of renal artery NOS Multiple renal arteries
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Artères rénales multiples Malformation congénitale de l'artère rénale SAI
WORLD HEALTH ORGANIZATION ICD-10: Q27.2
WORLD HEALTH ORGANIZATION ICD-10: Q27.2
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]


Others have searched : congenital anomaly    multiple congenital exostoses    nos of brain    amyoplasia congenita    arthrogryposis multiplex congenita    congenital multiple arthrogryposis    deformity    disease or lesion    multiple anomalies    myodystrophia fetalis    


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'congenital multiple arthrogryposis'

Date index:2021-04-19 -

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