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ARPKD
Atrophy of kidney
Atrophy of kidney congenital
Autosomal dominant polycystic kidney disease
Cerebellar congenital atrophy
Congenital absence of kidney
Congenital cystic kidney
Congenital polycystic disease
Congenital solitary kidney
Cyst of kidney
Infantile
Polycystic disease of kidneys
Polycystic kidney
Polycystic kidney disease
Polycystoma of the kidney
Unilateral renal agenesis

Translation of "Atrophy kidney congenital " (English → French) :

polycystic kidney | polycystic disease of kidneys | congenital cystic kidney | polycystoma of the kidney
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
maladie kystique des reins | reins polykystiques | reins polymicrokystiques | polykystome rénal | maladie polykystique des reins | polykystose rénale
médecine
médecine
http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]
http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]
atrophy of kidney:congenital | infantile | congenital absence of kidney
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
absence congénitale de rein(s) atrophie rénale:congénitale | infantile
WORLD HEALTH ORGANIZATION ICD-10: Q60
WORLD HEALTH ORGANIZATION ICD-10: Q60
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
Cyst of kidney (congenital)(single)
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Kyste du rein (congénital) (unique)
WORLD HEALTH ORGANIZATION ICD-10: Q61.0
WORLD HEALTH ORGANIZATION ICD-10: Q61.0
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
autosomal dominant polycystic kidney disease | congenital polycystic disease | polycystic kidney disease | ARPKD [Abbr.]
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
polykystose rénale | PKR [Abbr.]
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
unilateral renal agenesis [ congenital absence of kidney ]
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
agénésie rénale unilatérale
Genitourinary Tract
Appareil génito-urinaire
http://www.btb.termiumplus.gc. (...) (...) [HTML] [2018-01-01]
http://www.btb.termiumplus.gc. (...) [HTML] [2018-01-01]
congenital solitary kidney
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
rein unique | rein unique congénital
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
cerebellar congenital atrophy
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
atrophie cérébelleuse congénitale
IATE - Health
IATE - Health
http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]
http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]
Depressions in skull Deviation of nasal septum, congenital Hemifacial atrophy or hypertrophy Squashed or bent nose, congenital
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
Atrophie ou hypertrophie hémifaciale Dépressions des os du crâne Déviation congénitale de la cloison nasale Ecrasement ou déviation congénital(e) du nez
WORLD HEALTH ORGANIZATION ICD-10: Q67.4
WORLD HEALTH ORGANIZATION ICD-10: Q67.4
https://icd.who.int/browse10/2 (...) (...) [HTML] [2018-01-01]
https://icd.who.int/browse10/2 (...) [HTML] [2018-01-01]
An extremely rare inborn error of sterol biosynthesis with manifestations of facial dysmorphism, congenital anomalies (including limb and kidney anomalies), failure to thrive, developmental delay and liver disease. Only 4 cases have been reported in
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
lathostérolose
SNOMEDCT-BE (including limb and kidney anomalies), failure to thrive, developmental delay and liver disease. Only 4 cases have been reported in / 719257008
SNOMEDCT-BE (disorder) / 719257008
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]
Atrophy of kidney
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
atrophie d'un rein
SNOMEDCT-BE (disorder) / 197659005
SNOMEDCT-BE (disorder) / 197659005
https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]
https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]


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'Atrophy kidney congenital'

Date index:2021-02-02 -

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