autosomal dominant polycystic kidney disease

autosomal dominant polycystic kidney disease
(ADPKD) see polycystic kidney d.

Medical dictionary. 2011.

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  • Polycystic kidney disease — Classification and external resources Polycystic kidneys ICD 10 Q …   Wikipedia

  • Polycystic kidney disease 2 — (autosomal dominant), also known as PKD2, is a human gene.cite web | title = Entrez Gene: PKD2 polycystic kidney disease 2 (autosomal dominant)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=5311|… …   Wikipedia

  • Polycystic kidney disease — Genetic disorder characterized by the development of innumerable cysts in the kidneys. These cysts are filled with fluid, and replace much of the mass of the kidneys. This reduces kidney function, leading to kidney * * * polycystic kidney disease …   Medical dictionary

  • Polycystic kidney disease 1 — Schematische Darstellung von Polycystin 1 und Polycystin 2 an einer Zelle.[1] PKD1 (engl. Abk. für polycystic kidney disease 1 (autosomal dominant) = „polyzystische Nierenerkrankung 1 (autosomal dominant)“) ist ein Gen, das sowohl beim Menschen… …   Deutsch Wikipedia

  • polycystic kidney disease — noun kidney disease characterized by enlarged kidneys containing many cysts; often leads to kidney failure • Syn: ↑PKD • Hypernyms: ↑kidney disease, ↑renal disorder, ↑nephropathy, ↑nephrosis * * * noun : either of two he …   Useful english dictionary

  • Cystic kidney disease — Classification and external resources ICD 10 Q61 ICD 9 753.1 …   Wikipedia

  • polycystic liver disease — any of several congenital conditions in which the liver develops cysts and sometimes Meyenburg complexes, often in association with polycystic kidney disease. An autosomal recessive type develops in childhood and can be rapidly fatal; an… …   Medical dictionary

  • Medullary cystic kidney disease — Classification and external resources ICD 9 753.16 OMIM 174000 603860 …   Wikipedia

  • Autosomal-dominante polyzystische Nierenerkrankung — Klassifikation nach ICD 10 Q61.1 Polyzystische Niere, autosomal rezessiv infantiler Typ Q61.2 Polyzystische Niere, autosomal dominant Erwachsenentyp …   Deutsch Wikipedia

  • Autosomal-rezessive polyzystische Nierenerkrankung — Klassifikation nach ICD 10 Q61.1 Polyzystische Niere, autosomal rezessiv infantiler Typ Q61.2 Polyzystische Niere, autosomal dominant Erwachsenentyp …   Deutsch Wikipedia

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