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 ]

This is just here as a test because I lose it

Term information

database cross reference
  • GARD:0009457 (Orphanet-shared)
  • OMIMPS:174050 (MONDO:equivalentTo)
  • HP:0006557 (MONDO:otherHierarchy)
  • DOID:0050770 (MONDO:equivalentTo)
  • NCIT:C82833 (MONDO:equivalentTo)
  • ICD9:751.62 (i2s)
  • SCTID:72925005 (MONDO:equivalentTo)
  • UMLS:C0158683 (NCIT:C82833)
definition

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

exactMatch

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

http://identifiers.org/snomedct/72925005

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

http://identifiers.org/mesh/C536330

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

has exact synonym

AD polycystic liver disease

ADPLD

polycystic liver disease

PCLD

has related synonym

fibrocystic liver disease

congenital cystic liver disease

congenital hepatic cyst

id

MONDO:0000447

seeAlso

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

should conform to

http://purl.obolibrary.org/obo/mondo/patterns/OMIM_phenotypic_series.yaml

Term relations