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ARPKD
Atrophy of kidney congenital
Autosomal dominant polycystic kidney disease
Cerebellar congenital atrophy
Congenital absence of kidney
Congenital atrophy of kidney
Congenital polycystic disease
Cyst of kidney
Infantile
Polycystic kidney disease

Traduction de «atrophy kidney congenital » (Anglais → Néerlandais) :

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

atrofie van nier | congenitaal | atrofie van nier | infantiel | congenitaal ontbreken van nier


A rare distal hereditary motor neuropathy with a variable clinical phenotype and typical characteristics of congenital, non-progressive, predominantly distal lower limb muscle weakness and atrophy and congenital (or early-onset) flexion contractures

autosomaal dominante congenitale benigne spinale spieratrofie


Cyst of kidney (congenital)(single)

niercyste (congenitaal)(solitair)


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

cystennier | polycystose renis | polycystosis renis | ren cysticus




cerebellar congenital atrophy

congenitale cerebellumatrofie


A rare mitochondrial disease with marked clinical variability typically and characteristics of encephalomyopathy, kidney disease (nephrotic syndrome), optic atrophy, early-onset deafness, pancytopenia, obesity, and cardiac disease (valvulopathy). Add

syndroom van doofheid, encefaloneuropathie, obesitas en klepinsufficiëntie


Depressions in skull Deviation of nasal septum, congenital Hemifacial atrophy or hypertrophy Squashed or bent nose, congenital

depressies in schedel | deviatie van neustussenschot, congenitaal | hemifaciale atrofie of hypertrofie | ingedeukte of kromme neus, congenitaal




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Date index: 2024-03-17
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