Cell Culture Ontology

Last uploaded: July 23, 2014
Preferred Name

cirrhosis, familial
Synonyms

cirrhosis, Noncryptogenic, susceptibility to

cirrhosis, cryptogenic

cirrhosis, familial, with pulmonary hypertension

Sen syndrome

endemic Tyrolean infantile cirrhosis

copper toxicosis, idiopathic

Indian childhood cirrhosis

copper-overload cirrhosis

hereditary cirrhosis of liver

cryptogenic cirrhosis

cirrhosis, familial

Definitions

Cirrhosis in which no causative agent can be identified.

ID

http://purl.obolibrary.org/obo/MONDO_0007329

database_cross_reference

UMLS:C1861556

OMIM:215600

NCIT:C84411

MESH:C566123

MEDGEN:350049

SCTID:6183001

definition

Cirrhosis in which no causative agent can be identified.

has_exact_synonym

hereditary cirrhosis of liver

cryptogenic cirrhosis

cirrhosis, familial

has_related_synonym

cirrhosis, Noncryptogenic, susceptibility to

cirrhosis, cryptogenic

cirrhosis, familial, with pulmonary hypertension

Sen syndrome

endemic Tyrolean infantile cirrhosis

copper toxicosis, idiopathic

Indian childhood cirrhosis

copper-overload cirrhosis

id

MONDO:0007329

in_subset

http://purl.obolibrary.org/obo/mondo/mondo-base#rare

http://purl.obolibrary.org/obo/mondo/mondo-base#otar

http://purl.obolibrary.org/obo/mondo/mondo-base#gard_rare

http://purl.obolibrary.org/obo/mondo/mondo-base#nord_rare

label

cirrhosis, familial

notation

MONDO:0007329

preferred label

cirrhosis, familial

prefLabel

cirrhosis, familial

skos_exactMatch

http://identifiers.org/snomedct/6183001

http://purl.obolibrary.org/obo/NCIT_C84411

http://identifiers.org/mesh/C566123

http://identifiers.org/medgen/350049

http://linkedlifedata.com/resource/umls/id/C1861556

https://omim.org/entry/215600

subClassOf

http://www.ebi.ac.uk/efo/EFO_0000508

http://www.ebi.ac.uk/efo/EFO_0001422

http://purl.obolibrary.org/obo/MONDO_0100137

Delete Subject Author Type Created
No notes to display