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Albright hereditary osteodystrophy
Alport's syndrome
Chronic familial erythremia
Cooley's anemia
Cooley's syndrome
Cooley's-disease
Cooley-Lee syndrome
Dameshek's syndrome
Erythroblastic anemia
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 disposition
Hereditary enemy
Hereditary foe
Hereditary gingival fibromatosis
Hereditary hyperplasia of the gingiva
Hereditary leptocytosis
Hereditary nephropathy
Hereditary nephropathy with haematuria
Hereditary predisposition
Mediterranean anemia
Mediterranean disease
Primary erythroblastic anemia
Target cell anemia
Target-oval cell syndrome
Thalassaemia major
Thalassemia major
Thalassemic syndrome

Traduction de «Hereditary leptocytosis » (Anglais → Français) :



Cooley's anemia | Cooley's-disease | Cooley's syndrome | Cooley-Lee syndrome | Dameshek's syndrome | chronic familial erythremia | erythroblastic anemia | hereditary leptocytosis | Mediterranean anemia | Mediterranean disease | primary erythroblastic anemia | target cell anemia | target-oval cell syndrome | thalassaemia major | thalassemia major | thalassemic syndrome

maladie de Cooley | anémie de Cooley | anémie érythroblastique familiale primitive | anémie méditerranéenne | anémie microcytaire familiale | érythrémie chronique familiale | hémo-ostéopathie de Cooley | leptocytose héréditaire | maladie méditerranéenne | syndrome de Cooley-Lee | thalassanémie | thalassémie érythroblastique familiale génotypique | thalassémie majeure | anémie érythrémique


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 foe [ hereditary enemy ]

ennemi héréditaire


hereditary hyperplasia of the gingiva | hereditary gingival fibromatosis | fibromatosis gingivae

hyperplasie gingivale congénitale diffuse | fibromatose idiopathique | éléphantiasis gingival | hyperplasie gingivale idiopathique


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


Albright hereditary osteodystrophy

ostéodystrophie héréditaire d'Albright


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