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Caroli Disease is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Caroli Disease, or a subtype of Caroli Disease,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Ophanet, a consortium of European partners,
currently defines a condition rare when it affects 1 person per 2,000.
They list Caroli Disease as a "rare disease".
Source - Orphanet
Complications of Caroli Disease:
see complications of Caroli Disease
Symptoms of Caroli Disease: see symptoms of Caroli Disease
Complications of Caroli Disease: see complications of Caroli Disease
Treatments for Caroli Disease:
see treatments for Caroli Disease
Research for Caroli Disease:
see research for Caroli Disease
Main name of condition: Caroli Disease
Other names or spellings for Caroli Disease:congenital biliary ectasias, acute cholangitis, congenital dilatation of intrahepatic bile ducts, Congenital polycystic dilatation of intrahepatic bile ducts, Caroli disease isolated, Cystic dilatation of the intrahepatic biliary tree
Congenital dilatation of lobar intrahepatic bile duct
Source - Diseases Database
Caroli disease isolated, Congenital polycystic dilatation of intrahepatic bile ducts, Cystic dilatation of the intrahepatic biliary tree
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)
Research the causes of these diseases that are similar to, or related to, Caroli Disease:
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