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Traduction de «hereditary familial hypogonadism » (Anglais → Français) :

Reifenstein's syndrome | hereditary familial hypogonadism

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

syndrome de Reifenstein | hypoilial héréditaire

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

hereditary familial pancreatitis

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pancréatite familiale héréditaire

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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

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

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http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

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ataxie de Friedreich [ maladie de Friedreich | ataxie héréditaire ]

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A hereditary renal cancer syndrome defined as development of hereditary clear cell renal cell carcinoma (ccRCC) in two or more family members without evidence of constitutional chromosome 3 translocation, von Hippel-Lindau disease or other neoplasm p

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carcinome rénal héréditaire à cellules claires

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hereditary hypophosphatemic rickets [ familial hypophosphatemic rickets | renal hypophosphatemia | familial hypophosphatemia ]

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rachitisme hypophosphatémique héréditaire

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hereditary spastic paraplegia [ HSP | familial spastic paralysis | Strümpell's disease ]

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paraplégie spastique familiale [ maladie de Strümpell-Lorrain | paraplégie spasmodique familiale de Strümpell-Lorrain ]

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http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) (...) [HTML] [2018-01-01]

http://gdt.oqlf.gouv.qc.ca/fic (...) [HTML] [2018-01-01]

This syndrome is characterized by primary hypergonadotropic hypogonadism and partial alopecia. So far, it has been described in seven patients from three families. Mullerian hypoplasia, absent or streak ovaries, hypoplastic internal genitalia and pri

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syndrome d'hypogonadisme hypergonadotrope primaire-alopécie partielle

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A very rare hereditary skin disease with manifestation of irregularly distributed epidermal hyperkeratosis of the palms and soles. Reported in 35 families worldwide to date. The lesions usually start to develop in early adolescence but can also prese

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kératodermie palmoplantaire ponctuée type 1

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D'autres ont cherché : alport's syndrome cooley's anemia cooley's syndrome cooley's-disease cooley-lee syndrome dameshek's syndrome 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 mediterranean anemia mediterranean disease reifenstein's syndrome strümpell's disease chronic familial erythremia erythroblastic anemia familial hereditary nephropathy familial hypophosphatemia familial hypophosphatemic rickets familial spastic paralysis haematuric familial nephropathy hereditary familial hypogonadism hereditary familial pancreatitis hereditary hypophosphatemic rickets hereditary leptocytosis hereditary nephropathy hereditary nephropathy with haematuria hereditary spastic paraplegia primary erythroblastic anemia renal hypophosphatemia target cell anemia target-oval cell syndrome thalassaemia major thalassemia major thalassemic syndrome

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Date index: 2021-06-10