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

SNOMEDCT-CA (ccRCC) in two or more family members without evidence of constitutional chromosome 3 translocation, von Hippel-Lindau disease or other neoplasm p / 764961009

SNOMEDCT-CA (trouble) / 764961009

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Syndrome:Peutz-Jeghers | Sturge-Weber(-Dimitri) | von Hippel-Lindau

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Syndrome de:Peutz-Jeghers | Sturge-Weber(-Dimitri) | von Hippel-Lindau

WORLD HEALTH ORGANIZATION ICD-10: Q85.8

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cerebroretinal angiomatosis | von Hippel-Lindau disease | von Hippel-Lindau syndrome | VHL [Abbr.]

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angiomatose rétinocérébelleuse | angiomatose rétinocérébelleuse de von Hippel-Lindau | maladie de Hippel-Lindau | syndrome de von Hippel-Lindau

IATE - Health

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Others have searched : sturge-weber vhl gene cerebroretinal angiomatosis von hippel-lindau von hippel-lindau disease von hippel-lindau gene von hippel-lindau syndrome Von Hippel-Lindau gene

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'Von Hippel-Lindau gene'

Date index:2021-05-07 -

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Translation of "Von Hippel-Lindau gene " (English → French) :

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