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Hepatic Fibrosis, Congenital MeSH Supplementary Concept Data 2024


MeSH Supplementary
Hepatic Fibrosis, Congenital
Unique ID
C562378
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C562378
Entry Term(s)
Congenital Fibrose Liver
Congenital Hepatic Fibrosis
Heading Mapped to
*Liver Cirrhosis
*Genetic Diseases, Inborn
Frequency
88
Note
associated with autosomal recessive polycystic kidney disease
Date of Entry
2012/11/05
Revision Date
2015/08/18
Hepatic Fibrosis, Congenital Preferred
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