Decreased liver function

Symptom Information:

Symptom ID: HPO:0001410
Synonyms:
Liver dysfunction [HPO:0001410]
LIVER DYSFUNCTION, MILD [HPO:0001410]
Liver functional anomaly [Orphanet:29000]
Hepatocellular liver disease [Orphanet:29240]
Decreased liver function [OMIM:Decreased liver function]
Liver dysfunction [OMIM:Liver dysfunction]
Liver dysfunction, mild [OMIM:Liver dysfunction, mild]
Functional anomalies of the liver and the biliary tract [Orphanet:29000]
Hepatocellular liver disease/hepatic failure [Orphanet:29240]
Liver dysfunction (in some patients) [OMIM:Liver dysfunction (in some patients)]
Liver dysfunction (less common) [OMIM:Liver dysfunction (less common)]
Quality:
Cross references:
Orphanet:29000 "Functional anomalies of the liver and the biliary tract" [Orphanet:29000]
Orphanet:29240 "Hepatocellular liver disease/hepatic failure" [Orphanet:29240]
OMIM: "Decreased liver function" [OMIM:Decreased liver function]
OMIM: "Liver dysfunction" [OMIM:Liver dysfunction]
OMIM: "Liver dysfunction, mild" [OMIM:Liver dysfunction, mild]
OMIM: "Liver dysfunction (in some patients)" [OMIM:Liver dysfunction (in some patients)]
OMIM: "Liver dysfunction (less common)" [OMIM:Liver dysfunction (less common)]
Is a (Direct Parents):
HPO         Abnormality of the liver
Orphanet Hepatic failure
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of the abdomen(HPO:0001438)
          Abnormality of the abdominal organs(HPO:0002012)
             Abnormality of the liver(HPO:0001392)
                Decreased liver function(HPO:0001410)
MedDRA:
Database Frequency: 59 / 7739
Resource:

All diseases associated with this symptom:

Alpers syndrome (Orphanet:726)
Alström syndrome (Orphanet:64)
Arthrogryposis - renal dysfunction - cholestasis (Orphanet:2697)
Bardet-Biedl syndrome (Orphanet:110)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Blau syndrome (Orphanet:90340)
Cirrhosis-dystonia-polycythemia-hypermanganesemia syndrome (Orphanet:309854)
Citrullinemia type I (Orphanet:247525)
Classic galactosemia (Orphanet:79239)
Combined oxidative phosphorylation defect type 11 (Orphanet:324535)
Combined oxidative phosphorylation defect type 9 (Orphanet:319509)
Congenital bile acid synthesis defect type 1 (Orphanet:79301)
Congenital bile acid synthesis defect type 2 (Orphanet:79303)
Congenital bile acid synthesis defect type 3 (Orphanet:79302)
Congenital disorder of glycosylation (Orphanet:137)
Congenital intrauterine infection-like syndrome (Orphanet:1229)
Crigler-Najjar syndrome (Orphanet:205)
Crigler-Najjar syndrome type 1 (Orphanet:79234)
DDOST-CDG (Orphanet:300536)
Disorder of bile acid synthesis (Orphanet:79168)
FADD-related immunodeficiency (Orphanet:306550)
Hemochromatosis type 2 (Orphanet:79230)
Hemochromatosis type 3 (Orphanet:225123)
Hemochromatosis, type 1 (OMIM:235200)
Hemochromatosis, type 2A (OMIM:602390)
Hemochromatosis, type 2B (OMIM:613313)
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 (Orphanet:137681)
Hereditary hemorrhagic telangiectasia (Orphanet:774)
Hyperbiliverdinemia (Orphanet:276405)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
Hyperornithinemia-hyperammonemia-homocitrullinuria (Orphanet:415)
INFANTILE LIVER FAILURE SYNDROME 2 (OMIM:615486)
Idiopathic copper-associated cirrhosis (Orphanet:209919)
Isolated CoQ-cytochrome C reductase deficiency (Orphanet:1460)
Isolated cytochrome C oxidase deficiency (Orphanet:254905)
Kawasaki disease (Orphanet:2331)
LIPOYLTRANSFERASE 1 DEFICIENCY (OMIM:616299)
MEDIUM CHAIN 3-KETOACYL-CoA THIOLASE DEFICIENCY (OMIM:602199)
MELAS (Orphanet:550)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Navajo neurohepatopathy (Orphanet:255229)
Neonatal hemochromatosis (Orphanet:446)
Nephronophthisis 15 (OMIM:614845)
Ornithine transcarbamylase deficiency (Orphanet:664)
PATENT DUCTUS VENOSUS (OMIM:601466)
PEROXISOME BIOGENESIS DISORDER 11A (ZELLWEGER) (OMIM:614883)
PEROXISOME BIOGENESIS DISORDER 5B (OMIM:614867)
PEROXISOME BIOGENESIS DISORDER 6B (OMIM:614871)
PEROXISOME BIOGENESIS DISORDER 7B (OMIM:614873)
PEROXISOME BIOGENESIS DISORDER 8B (OMIM:614877)
Pyruvate dehydrogenase E3 deficiency (Orphanet:2394)
Renal cysts and diabetes syndrome (Orphanet:93111)
Renal tubulopathy - encephalopathy - liver failure (Orphanet:254902)
Rotor syndrome (Orphanet:3111)
STT3B-CDG (Orphanet:370924)
Short chain acyl-CoA dehydrogenase deficiency (Orphanet:26792)
Transaldolase deficiency (Orphanet:101028)
Wilson disease (Orphanet:905)
X-linked centronuclear myopathy (Orphanet:596)