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ARPKD
Atrophy of kidney congenital
Autosomal dominant polycystic kidney disease
Congenital absence of kidney
Congenital cyst of kidney
Congenital cystic kidney
Congenital displaced kidney Malrotation of kidney
Congenital polycystic disease
Congenital solitary kidney
Infantile
Polycystic disease of kidneys
Polycystic kidney
Polycystic kidney disease
Polycystoma of the kidney
Unilateral renal agenesis

Traduction de «congenital solitary kidney » (Anglais → Français) :

congenital solitary kidney

rein unique | rein unique congénital


polycystic kidney | polycystic disease of kidneys | congenital cystic kidney | polycystoma of the kidney

maladie kystique des reins | reins polykystiques | reins polymicrokystiques | polykystome rénal | maladie polykystique des reins | polykystose rénale


Congenital displaced kidney Malrotation of kidney

Déplacement congénital du rein Malrotation du rein


autosomal dominant polycystic kidney disease | congenital polycystic disease | polycystic kidney disease | ARPKD [Abbr.]

polykystose rénale | PKR [Abbr.]


unilateral renal agenesis [ congenital absence of kidney ]

agénésie rénale unilatérale


atrophy of kidney:congenital | infantile | congenital absence of kidney

absence congénitale de rein(s) atrophie rénale:congénitale | infantile


Cyst (multiple)(solitary) of kidney, acquired

Kyste du rein (multiple) (solitaire), acquis


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

lathostérolose


A rare multiple congenital anomalies/dysmorphic syndrome with characteristics of male, 46,XY gonadal dysgenesis, cleft palate, micrognathia, conotruncal heart defects and unspecific skeletal, brain and kidney anomalies.

syndrome génito-palato-cardiaque


Congenital cyst of kidney

polykystose rénale congénitale


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