hepatic fibrosis, congenital

Preferred Label : hepatic fibrosis, congenital;

MeSH note : associated with autosomal recessive polycystic kidney disease;

MeSH synonym : Congenital Fibrose Liver; Congenital Hepatic Fibrosis;

Details

Origin ID

C562378;

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 [NCIt concept]
- Congenital hepatic fibrosis [ICD-11 More detail]
- Congenital hepatic fibrosis [HPO term]
- Congenital hepatic fibrosis [MedDRA Preferred Term]
- Congenital hepatic fibrosis [HRDO Sign]
- Congenital hepatic fibrosis (disorder) [SNOMED CT concept]
- congenital hepatic fibrosis [Radlex concept]
- congenital hepatic fibrosis [SNOMED Notion]
HPO term
- Congenital hepatic fibrosis [HPO term]
MeSH term(s) associated for indexing
- genetic diseases, inborn [MeSH Descriptor]
- liver cirrhosis [MeSH Descriptor]
Record concept(s)
- hepatic fibrosis, congenital [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Congenital Hepatic Fibrosis [NCIt 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]

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