about
acute liver failurecholangiolocellular carcinomaacute fatty liver of pregnancyacute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndromeFamilial cirrhosisferro-cerebro-cutaneous syndromehepatic fibrosis-renal cysts-intellectual disability syndromeacute infantile liver failure due to synthesis defect of mtDNA-encoded proteinstransient infantile hypertriglyceridemia and hepatosteatosisfever-associated acute infantile liver failure syndromepulmonary fibrosis-hepatic hyperplasia-bone marrow hypoplasia syndromeFulminant viral hepatitisgrowth retardation-mild developmental delay-chronic hepatitis syndromeCirrhotic cardiomyopathyIgG4-related hepatopathyautoimmune hepatitis
P279
Q1192530-4634EEB3-621B-44F4-9773-16056360088EQ18557684-5F5A1349-C7C0-4260-9651-2DD5C8BC5EE3Q4677929-C77EEBF5-CE0E-4C65-9AFD-547817BDFD2DQ50349821-D4535018-6C91-447E-ACA1-A663BD01C28CQ5432933-E3EAB0A9-7DDB-4541-9ECC-A308232FAE73Q55346037-0D02C381-D758-4C7A-BD27-3A501649A9B0Q55781732-4085707F-C670-4E7A-89C7-F76EDF4F144CQ55783956-716A81C6-2478-4571-A461-C5D02BF3EF7BQ55784334-B06757ED-4D0F-4FFF-9B04-4F50FC2262F5Q55784921-BD7E99DA-FBCC-4FEB-8162-CFE663D5208BQ55786063-B02CE0DC-CCFC-4993-B462-78C40CBC93C5Q55787743-8C807DD9-710A-4698-8334-8FE18731A107Q55787952-AF3097B4-7B4D-4744-9FD4-6750602361E8Q55788411-E3B0C034-EBF4-45FC-8F07-BBEAD3E7FBBCQ55788705-76E798EF-29D1-49D8-9ED0-ADF91E2FAA46Q786844-06DD307A-D280-44E8-8D25-841945910E65
P279
description
human disease
@en
name
rare parenchymal liver disease
@en
type
label
rare parenchymal liver disease
@en
prefLabel
rare parenchymal liver disease
@en
P1550
P2888
P5270
MONDO:0015114