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Congenital long QT syndrome
Congenital nephrosis
Congenital nephrotic syndrome
Familial congenital hypokaliaemia
Familial long QT syndrome
Familial nephrosis
Infants
Inherited long QT syndrome
LQTS
Long QT Syndrome
Long QT syndrome
Primary

Traduction de «Familial congenital hypokaliaemia » (Anglais → Français) :

familial congenital hypokaliaemia
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
hypokaliémie alcalosique congénitale
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
congenital nephrosis | familial nephrosis | congenital nephrotic syndrome
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
syndrome néphrotique congénital du nouveau-né
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
long QT syndrome | LQTS | Long QT Syndrome | familial long QT syndrome | congenital long QT syndrome | inherited long QT syndrome
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
syndrome du QT long congénital | syndrome du QTL | syndrome du QT long
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
A very rare congenital malformation of the digits with the absence of the middle phalanges (usually of digits two to five), nail dysplasia and duplicated terminal phalanx of the thumb. Has been described in patients from two unrelated families.
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
brachydactylie type A5
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
A very rare multiple congenital anomalies syndrome described in three brothers of one South-African family, and with features of hypospadias and intellectual deficit, in association with microcephaly, craniofacial dysmorphism, joint laxity and beaked
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome d'hypospadias-déficience intellectuelle type Goldblatt
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
A very rare syndrome described in three siblings of one Japanese family with main features of congenital heart disease, round face with depressed nasal bridge, small mouth, short stature, and relatively dark skin and typical dermatoglyphic anomalies,
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
syndrome de cardiopathie congénitale-face ronde-petite taille
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Family history of congenital malformations, deformations and chromosomal abnormalities
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Antécédents familiaux de malformations congénitales et anomalies chromosomiques
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [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]
Acholuric (familial) jaundice Congenital (spherocytic) haemolytic icterus Minkowski-Chauffard syndrome
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Ictère:acholurique (familial) | hémolytique congénital (sphérocytaire) | Syndrome de Minkowski-Chauffard
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]


D'autres ont cherché : long qt syndrome     congenital long qt syndrome     congenital nephrosis     congenital nephrotic syndrome     familial congenital hypokaliaemia     familial long qt syndrome     familial nephrosis     infants     inherited long qt syndrome     primary     Familial congenital hypokaliaemia     


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Date index: 2021-12-09
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