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| Term | Caroli syndrome | ID (Ontology) | DOID:0081394 (Human Disease) |
| Definition | A syndrome that is characterized by the presence of associated congenital hepatic fibrosis and that is associated with autosomal recessive polycystic kidney disease. | ||
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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autosomal genetic disease |__autosomal recessive disease__ vascular disease | |__hepatic vascular disease_____| |__vein disease_________________| disease | liver disease | |__hepatic vascular disease_____| |__syndrome_____________________| biliary tract disease | |__bile duct disease____________| Caroli syndrome |
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| Is a |
autosomal recessive disease syndrome hepatic vascular disease bile duct disease vein disease |
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External Crossreferences & Linkouts
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| GARD:6002 | |||