(autosomal recessive polycystic kidney disease)
1autosomal recessive polycystic kidney disease — (ARPKD) see polycystic kidney d …
2Polycystic kidney disease — Classification and external resources Polycystic kidneys ICD 10 Q …
3Polycystic 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 …
4polycystic 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 …
5Cystic kidney disease — Classification and external resources ICD 10 Q61 ICD 9 753.1 …
6polycystic 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… …
7Medullary cystic kidney disease — Classification and external resources ICD 9 753.16 OMIM 174000 603860 …
8Autosomal-dominante polyzystische Nierenerkrankung — Klassifikation nach ICD 10 Q61.1 Polyzystische Niere, autosomal rezessiv infantiler Typ Q61.2 Polyzystische Niere, autosomal dominant Erwachsenentyp …
9Autosomal-rezessive polyzystische Nierenerkrankung — Klassifikation nach ICD 10 Q61.1 Polyzystische Niere, autosomal rezessiv infantiler Typ Q61.2 Polyzystische Niere, autosomal dominant Erwachsenentyp …
10Autosomal dominante polyzystische Nierenerkrankung — Klassifikation nach ICD 10 Q61.1 Polyzystische Niere, autosomal rezessiv infantiler Typ Q61.2 Polyzystische Niere, autosomal dominant Erwachsenentyp …
