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autosomal dominant polycystic liver disease

^ http://purl.obolibrary.org/obo/MONDO_0000447

An autosomal dominant inherited condition characterized by many cysts of various sizes scattered throughout the liver. [ GARD:0009457 ]

Term info

database cross reference
  • MedDRA:10048834 (MONDO:relatedTo)
  • ICD10CM:Q44.6 (MONDO:equivalentTo)
  • HP:0006557 (MONDO:otherHierarchy)
  • OMIMPS:174050 (MONDO:equivalentTo)
  • ICD9:751.62 (MONDO:i2s)
  • Orphanet:2924 (MONDO:equivalentTo)
  • MedDRA:10010427 (MONDO:relatedTo)
  • SCTID:72925005 (MONDO:equivalentTo)
  • NCIT:C82833 (MONDO:equivalentTo)
  • UMLS:C0158683 (NCIT:C82833)
  • GARD:0009457 (MONDO:equivalentTo)
  • MedDRA:10083939
  • DOID:0050770 (MONDO:equivalentTo)
definition

An autosomal dominant inherited condition characterized by many cysts of various sizes scattered throughout the liver.

exactMatch

https://omim.org/phenotypicSeries/PS174050, http://purl.obolibrary.org/obo/NCIT_C82833, http://identifiers.org/snomedct/72925005, http://purl.obolibrary.org/obo/DOID_0050770, http://purl.obolibrary.org/obo/Orphanet_2924, http://purl.bioontology.org/ontology/ICD10CM/Q44.6, http://linkedlifedata.com/resource/umls/id/C0158683

has exact synonym

AD polycystic liver disease, ADPLD, isolated congenital polycystic liver disease, isolated polycystic liver disease, polycystic liver disease, PCLD

has related synonym

fibrocystic liver disease, congenital cystic liver disease, congenital hepatic cyst

id

MONDO:0000447

relatedMatch

http://identifiers.org/meddra/10010427, http://identifiers.org/meddra/10048834

seeAlso

https://rarediseases.info.nih.gov/diseases/9457/polycystic-liver-disease

Term relations