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Alport's syndrome
Amelogenesis imperfecta
Bessel-Hagen disease
Familial hereditary nephropathy
Fibromatosis gingivae
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
Hereditary amelogenesis imperfecta
Hereditary brown enamel
Hereditary chondrodysplasia
Hereditary deforming chondrodysplasia
Hereditary disposition
Hereditary enamel dysplasia
Hereditary enamel hypoplasia
Hereditary enemy
Hereditary foe
Hereditary gingival fibromatosis
Hereditary hyperplasia of the gingiva
Hereditary multiple exostosis
Hereditary nephropathy
Hereditary nephropathy with haematuria
Hereditary predisposition
Multiple cartilaginous exostoses
Multiple exostosis
Multiple osteochondromas
Spider lamb syndrome
Spider syndrome

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

spider syndrome [ spider lamb syndrome | hereditary chondrodysplasia ]

syndrôme de l'araignée [ chondrodysplasie 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 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 enamel dysplasia | amelogenesis imperfecta | hereditary amelogenesis imperfecta

dystrophie brune héréditaire de l'émail | amélogenèse imparfaite | hypoplasie brune héréditaire de l'émail


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


hereditary disposition | hereditary predisposition

disposition héréditaire | prédisposition héréditaire


hereditary brown enamel | hereditary enamel hypoplasia

mélanodontie


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


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