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autosomal dominant polycystic liver disease

Go to external page 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 ]

Synonyms: AD polycystic liver disease ADPLD isolated congenital polycystic liver disease isolated polycystic liver disease polycystic liver disease PCLD

This is just here as a test because I lose it

Term information

database cross reference
  • MedDRA:10083939
  • DOID:0050770 (MONDO:equivalentTo)
  • NCIT:C82833 (MONDO:equivalentTo)
  • ICD10CM:Q44.6 (MONDO:equivalentTo)
  • Orphanet:2924 (MONDO:equivalentTo)
  • MedDRA:10048834 (MONDO:relatedTo)
  • MedDRA:10010427 (MONDO:relatedTo)
  • HP:0006557 (MONDO:otherHierarchy)
  • OMIMPS:174050 (MONDO:equivalentTo)
  • SCTID:72925005 (MONDO:equivalentTo)
  • GARD:9457 (Orphanet:2924)
  • UMLS:C0158683 (NCIT:C82833)
  • ICD9:751.62 (MONDO:i2s)
Subsets

gard_rare, rare, orphanet_rare

exactMatch

https://omim.org/phenotypicSeries/PS174050

http://purl.obolibrary.org/obo/NCIT_C82833

http://www.orpha.net/ORDO/Orphanet_2924

http://identifiers.org/snomedct/72925005

http://purl.obolibrary.org/obo/DOID_0050770

http://linkedlifedata.com/resource/umls/id/C0158683

http://purl.bioontology.org/ontology/ICD10CM/Q44.6

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