Medical Subject Headings

Last uploaded: January 31, 2024

Preferred Name	Hepatic Fibrosis, Congenital
Synonyms	Congenital Fibrose Liver
ID	http://purl.bioontology.org/ontology/MESH/C562378
altLabel	Congenital Fibrose Liver Congenital Hepatic Fibrosis
cui	C0009714
HM	D008103 D030342
Inverse of RB	0
Mapped to	http://purl.bioontology.org/ontology/MESH/D030342 http://purl.bioontology.org/ontology/MESH/D008103
MDA	20121105
MeSH Frequency	88
MMR	20150818
notation	C562378
prefLabel	Hepatic Fibrosis, Congenital
SC	3
Scope Statement	associated with autosomal recessive polycystic kidney disease
TERMUI	T841180 T841179 T800578
TH	OMIM (2013) GHR (2014)
tui	T047

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Mapping To	Ontology	Source
http://purl.bioontology.org/ontology/MDRGER/10056533	MDRGER	CUI
http://purl.bioontology.org/ontology/OMIM/MTHU031839	OMIM	CUI
http://purl.bioontology.org/ontology/OMIM/MTHU075070	OMIM	CUI
http://purl.bioontology.org/ontology/OMIM/263200	OMIM	CUI
http://purl.bioontology.org/ontology/SCTSPA/79607001	SCTSPA	CUI
http://purl.bioontology.org/ontology/SNOMEDCT/79607001	SNOMEDCT	CUI
http://purl.bioontology.org/ontology/RCD/X307X	RCD	CUI
http://purl.bioontology.org/ontology/SNMI/D4-57450	SNMI	CUI
http://purl.bioontology.org/ontology/MEDDRA/10056533	MEDDRA	CUI
http://purl.bioontology.org/ontology/MDRFRE/10056533	MDRFRE	CUI
http://purl.bioontology.org/ontology/OMIM/MTHU031839	OMIM	LOOM
http://phenomebrowser.net/ontologies/mesh/mesh.owl#C562378	RH-MESH	LOOM