Disease | caroli disease |
Phenotype | C0085548|autosomal recessive polycystic kidney disease |
Sentences | 4 |
PubMedID- 21258203 | [caroli syndrome with autosomal recessive polycystic kidney disease]. |
PubMedID- 22626802 | The differential diagnoses of concomitant liver and renal disease in children may also include the following: (1) conditions sharing the same etiology, such as congenital hepatic fibrosis and caroli disease associated with autosomal recessive polycystic kidney disease,[13] (2) chronic viral infection, such as chronic hepatitis b causing membranous nephropathy,[14] or (3) renal impairment in a failing liver due to various causes, occurring as a terminal event, such as hepatorenal syndrome. |
PubMedID- 25447106 | autosomal recessive polycystic kidney disease with caroli syndrome. |
PubMedID- 24969198 | caroli's syndrome with autosomal recessive polycystic kidney disease. |
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