Term info
database cross reference
- ICD9:576.8 (MONDO:relatedTo)
- Orphanet:284385 (MONDO:equivalentTo)
- UMLS:CN227107 (MONDO:equivalentTo)
- UMLS:CN239338 (MONDO:equivalentTo)
- SCTID:74162007 (MONDO:equivalentTo)
Subsets
disease_grouping, ordo_group_of_disorders
definition
An instance of intrahepatic cholestasis that is caused by an inherited modification of the individual's genome.
exactMatch
http://identifiers.org/snomedct/74162007, http://purl.obolibrary.org/obo/Orphanet_284385, http://linkedlifedata.com/resource/umls/id/CN239338, http://linkedlifedata.com/resource/umls/id/CN227107
has exact synonym
hereditary intrahepatic cholestasis
id
MONDO:0017290