Vertaling van "Hereditary tyrosinaemia " (Engels → Frans) :

tyrosinaemia | hereditary tyrosinemia | tyrosinosis | hereditary tyrosinaemia | Baber's syndrome | atypical tyrosinosis | genuine tyrosyluria | hypermethioninaemia | inborn hepatorenal dysfunction
tyrosinémie | tyrosinémie héréditaire | tyrosinémie de type 1 | tyrosinose héréditaire | tyrosinose congénitale | tyrosinose

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 ]

hereditary hyperplasia of the gingiva | hereditary gingival fibromatosis | fibromatosis gingivae
hyperplasie gingivale congénitale diffuse | fibromatose idiopathique | éléphantiasis gingival | hyperplasie gingivale idiopathique

hereditary foe [ hereditary enemy ]
ennemi héréditaire

Bessel-Hagen disease | hereditary deforming chondrodysplasia | hereditary multiple exostosis | multiple cartilaginous exostoses | multiple exostosis | multiple osteochondromas
chondrodysplasie déformante héréditaire | maladie de Bessel-Hagen | maladie des exostoses multiples | maladie exostosante | maladie ostéogénique | ostéochondromes multiples

hereditary brown enamel | hereditary enamel hypoplasia
mélanodontie

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

Albright hereditary osteodystrophy
ostéodystrophie héréditaire d'Albright