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Alport's syndrome
Amyloidosis cutis
Amyloidosis of the liver
Amyloidosis of the skin
Familial hereditary nephropathy
Friedreich disease
Friedreich familial ataxia
Friedreich hereditary ataxia
Friedreich hereditary spinal ataxia
Friedreich spinocerebella
Friedreich's ataxia
Friedreich's disease
Friedreich's familial ataxia
Friedreich's hereditary ataxia
Friedreich's hereditary spinal ataxia
Haematuric familial nephropathy
Hepatic amyloidosis
Hereditary amyloidosis
Hereditary disposition
Hereditary enemy
Hereditary foe
Hereditary nephropathy
Hereditary nephropathy with haematuria
Hereditary predisposition
Liver amyloidosis

Traduction de «hereditary amyloidosis » (Anglais → Français) :



hereditary cerebral hemorrhage with amyloidosis of the Dutch type; HCHWA-Dutch

hémorragie cérébrale héréditaire avec amyloïdose de type hollandais


hepatic amyloidosis [ amyloidosis of the liver | liver amyloidosis ]

amyloïdose hépatique [ amylose hépatique | amyloïdose du foie ]


hereditary nephropathy | Alport's syndrome | hereditary haematuria associated with nerve deafness and ocular changes | hereditary hematuria associated with nerve deafness and ocular changes | hereditary nephropathy with haematuria | familial hereditary nephropathy | haematuric familial nephropathy

néphropathie familiale avec surdité | syndrome d'Alport | néphrite hématurique héréditaire avec surdité | néphrite chronique héréditaire


Friedreich's ataxia [ Friedreich's disease | Friedreich disease | Friedreich's hereditary spinal ataxia | Friedreich hereditary spinal ataxia | Friedreich familial ataxia | Friedreich's familial ataxia | Friedreich hereditary ataxia | Friedreich's hereditary ataxia | Friedreich spinocerebella ]

ataxie de Friedreich [ maladie de Friedreich | ataxie héréditaire ]


amyloidosis cutis | amyloidosis of the skin

amyloïdose cutanée


hereditary foe [ hereditary enemy ]

ennemi héréditaire


hereditary disposition | hereditary predisposition

disposition héréditaire | prédisposition héréditaire


An inherited group of small vessel diseases comprised of cerebroretinal vasculopathy (CRV), hereditary vascular retinopathy (HRV) and hereditary endotheliopathy with retinopathy, nephropathy and stroke all exhibiting progressive visual impairment as

vasculopathie rétinienne avec leucoencéphalopathie cérébrale et manifestations systémiques


Ovarian cancer caused by germline mutations in various genes, usually associated with additional cancer risks. The most common are breast and ovarian cancer syndrome (HBOC) due to mutations in BRCA1 and BRCA2 genes and hereditary nonpolyposis colorec

syndrome héréditaire de prédisposition au cancer de l'ovaire


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