Congenital Hepatic Fibrosis

Preferred Label : Congenital Hepatic Fibrosis;

NCIt definition : A congenital disorder usually inherited in an autosomal recessive pattern. It affects the hepatobiliary system and the kidneys. It is characterized by liver fibrosis, portal hypertension, and renal cysts.;

Détails

Origin ID

C97071;

UMLS CUI

C0009714;

Automatic exact mappings (from CISMeF team)
- Polycystic kidney disease 4 with or without polycystic liver disease [OMIM Phenotype]
Currated CISMeF NLP mapping
- Congenital hepatic fibrosis [HPO term]
- Congenital hepatic fibrosis [MedDRA Preferred Term]
- Congenital hepatic fibrosis [HRDO Sign]
- Congenital hepatic fibrosis [ICD-11 More detail]
- Congenital hepatic fibrosis (disorder) [SNOMED CT concept]
- congenital hepatic fibrosis [SNOMED Notion]
- congenital hepatic fibrosis [Radlex concept]
- hepatic fibrosis, congenital [MeSH concept]
- hepatic fibrosis, congenital [MeSH Supplementary Concept]
Has associated anatomic sites
- Digestive System [NCIt concept]
- Hepatobiliary System [NCIt concept]
- Liver [NCIt concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital hepatic fibrosis [MedDRA Preferred Term]
- Congenital hepatic fibrosis [HPO term]
- Congenital hepatic fibrosis [HRDO Sign]
- Congenital hepatic fibrosis (disorder) [SNOMED CT concept]
- congenital hepatic fibrosis [SNOMED Notion]
- congenital hepatic fibrosis [Radlex concept]
- hepatic fibrosis, congenital [MeSH Supplementary Concept]
- hepatic fibrosis, congenital [MeSH concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
disease_has_finding
- Congenital Lesion [NCIt concept]
disease_has_primary_anatomic_site
- Digestive System [NCIt concept]
- Hepatobiliary System [NCIt concept]
- Liver [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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