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Arnold-Chiari malformation
Cerebellar ectopia
Chiari malformation
Congenital absence of vertebra
Fusion of spine
Hemivertebra
Hereditary malformation
Herniation of the cerebellar tonsils
Hindbrain herniation
Infants
Kyphosis
Lordosis
Malformation of lumbosacral
Malformation of spine
Malformation of the bladder
Mondini's malformation
Platyspondylisis
Prenatal malformation
Primary
Supernumerary vertebra
Unspecified or not associated with scoliosis
Vesical malformation

Traduction de «Mondini's malformation » (Anglais → Français) :

Mondini's malformation
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
malformation de Mondini
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
Arnold-Chiari malformation | cerebellar ectopia | Chiari malformation | herniation of the cerebellar tonsils | hindbrain herniation
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
malformation d'Arnold-Chiari
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
hereditary malformation | prenatal malformation
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
malformation déficitaire
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
malformation of the bladder | vesical malformation
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
malformation vésicale
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
A unique form of congenital adrenal hyperplasia characterised by glucocorticoid deficiency, severe sexual ambiguity in both sexes and skeletal (especially craniofacial) malformations. Prenatal androgen excess is responsible for severe virilisation of
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
hyperplasie congénitale des surrénales par déficit en cytochrome P450 oxydoréductase
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
A rare chromosomal anomaly syndrome with a highly variable phenotype. Principle characteristics are intellectual disability, growth and developmental delay, facial dysmorphism (including microphthalmia, deep-set eyes, low-set, malformed ears, bulbous
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
trisomie 9 en mosaïque
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Congenital:absence of vertebra | fusion of spine | kyphosis | lordosis | malformation of lumbosacral (joint) (region) | Hemivertebra | Malformation of spine | Platyspondylisis | Supernumerary vertebra | unspecified or not associated with scoliosis
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Absence congénitale de vertèbres | Cyphose congénitale | Hémivertèbre [hémispondylie] | Lordose congénitale | Malformation congénitale (charnière) de la région lombo-sacrée | Malformation du rachis | Platyspondylie | Synostose vertébrale congénitale | Vertèbre surnuméraire | sans précision ou non associée à une scoliose
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
A rare genetic multiple congenital anomalies syndrome with characteristics of second branchial arch anomalies (branchial cysts and fistulae), malformations of the outer, middle and inner ear associated with sensorineural, mixed or conductive hearing
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome branchio-otique
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Aplasia, (pure) red cell (of):congenital | infants | primary | Blackfan-Diamond syndrome Familial hypoplastic anaemia Fanconi's anaemia Pancytopenia with malformations
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Anémie (de):Fanconi | hypoplasique familiale | Erythroblastopénie (pure) (du):congénitale | nourrisson | primaire | Pancytopénie avec malformations Syndrome de Blackfan-Diamond
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Meningeal haemorrhage Rupture of cerebral arteriovenous malformation
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Hémorragie méningée Rupture d'une malformation artérioveineuse cérébrale
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]


D'autres ont cherché : arnold-chiari malformation     chiari malformation     congenital absence of vertebra     hemivertebra     malformation of spine     mondini's malformation     platyspondylisis     supernumerary vertebra     cerebellar ectopia     fusion of spine     hereditary malformation     herniation of the cerebellar tonsils     hindbrain herniation     infants     kyphosis     lordosis     malformation of lumbosacral     malformation of the bladder     prenatal malformation     primary     vesical malformation     Mondini's malformation     


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Date index: 2022-06-05
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