Polycystic Liver Disease

Preferred Label : Polycystic Liver Disease;

NCIt definition : A usually asymptomatic hereditary disorder which is often associated with polycystic kidney disease. It is characterized by the presence of fluid-filled biliary cysts throughout the liver.;

Details

Origin ID

C82833;

UMLS CUI

C0158683;

Automatic exact mappings (from CISMeF team)
- Polycystic liver disease [ICD-11 Sub-sub category]
- Polycystic liver disease [OMIM phenotypic series]
Currated CISMeF NLP mapping
- Congenital cystic disease of liver (disorder) [SNOMED CT concept]
- Fibropolycystic liver disease [ICD-11 Sub-sub category]
- Isolated polycystic liver disease [ORDO Disease]
- Isolated polycystic liver disease (disorder) [SNOMED CT concept]
- Polycystic liver disease [HPO term]
- Polycystic liver disease [MedDRA Preferred Term]
- Polycystic liver disease [MeSH concept]
- congenital cystic disease of liver [MedDRA Preferred Term]
- polycystic liver [Disease (Nov.)]
- polycystic liver disease [DO Concept]
- polycystic liver disease [MeSH Supplementary Concept]
Has associated anatomic sites
- Digestive System [NCIt concept]
- Hepatobiliary System [NCIt concept]
- Liver [NCIt concept]
See also inter- (CISMeF)
- Fibropolycystic disease of liver (disorder) [SNOMED CT concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital cystic disease of liver (disorder) [SNOMED CT concept]
- Cystic disease of liver [ICD-10 Sub-category (who)]
- Cystic liver disease [HPO term]
- Isolated polycystic liver disease [ORDO Disease]
- Polycystic liver disease [MedDRA Preferred Term]
- Polycystic liver disease [MeSH concept]
- Polycystic liver disease [HPO term]
- congenital cystic disease of liver [SNOMED Notion]
- polycystic liver [Disease (Nov.)]
- polycystic liver disease [MeSH Supplementary Concept]
Validated automatic mappings to BTNT
- Polycystic liver disease 1 with or without kidney cysts [OMIM Phenotype]
disease_has_associated_gene
- MIR15A Gene [NCIt concept]
- MIR15A wt Allele [NCIt concept]
disease_has_finding
- Cystic Change [NCIt concept]
disease_has_primary_anatomic_site
- Digestive System [NCIt concept]
- Liver [NCIt concept]

Keyword's position in hierarchy(ies) :

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