FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term polycystic liver disease ID (Ontology) DOID:0050770 (Human Disease)
Definition A liver disease that is characterized by the presence of multiple cysts located_in the liver.
Also Known As "congenital cystic liver disease" ; "congenital hepatic cyst" ; "fibrocystic liver disease"
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Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
hepatobiliary disease           |
 |__liver disease_______________|
                                polycystic liver disease  6 rec.
                                 |__polycystic liver disease 1 2 rec.
                                 |__polycystic liver disease 2 1 rec.
                                 |__polycystic liver disease 3 1 rec.
                                 |__polycystic liver disease 4 2 rec.
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Is a autosomal dominant disease
liver disease
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Synonyms
  • "congenital cystic liver disease" EXACT
    "congenital hepatic cyst" EXACT
    "fibrocystic liver disease" EXACT
Secondary IDs
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GARD:9457
MESH:C536330