Hepatic steatosis

Symptom Information:

Symptom ID: HPO:0001397
Synonyms:
Fatty infiltration of liver [HPO:0001397]
Fatty liver [HPO:0001397]
Liver steatosis [HPO:0001397]
Steatosis [HPO:0001397]
Non-alcoholic fatty liver disease [Orphanet:29540]
Non-alcoholic fatty liver (disorder) [Orphanet:29540]
Nonalcoholic steatohepatitis (disorder) [Orphanet:29540]
Steatohepatitis (disorder) [Orphanet:29540]
Hepatic lipidosis [Orphanet:29540]
Fatty Liver [Orphanet:29540]
Non-alcoholic Fatty Liver Disease [Orphanet:29540]
Steatohepatitis [Orphanet:29540]
Fatty infiltration of liver [OMIM:Fatty infiltration of liver]
Fatty liver [OMIM:Fatty liver]
Hepatic steatosis [OMIM:Hepatic steatosis]
Liver steatosis [OMIM:Liver steatosis]
Steatosis [OMIM:Steatosis]
Liver/hepatic steatosis [Orphanet:29540]
Metamorphosis fatty liver [Orphanet:29540]
Non-alcoholic steatohepatitis [Orphanet:29540]
Hepatic steatosis [Orphanet:29540]
Liver fatty degeneration [Orphanet:29540]
Hepatic steatosis [MedDRA:10019708]
Acute fatty liver [MedDRA:10019708]
Degeneration fatty liver [MedDRA:10019708]
Fatty liver [MedDRA:10019708]
Fatty liver infiltration [MedDRA:10019708]
Fatty liver metamorphosis [MedDRA:10019708]
Hepatic macrosteatosis [MedDRA:10019708]
Hepatic microsteatosis [MedDRA:10019708]
Infiltration fatty liver [MedDRA:10019708]
Liver fatty [MedDRA:10019708]
Liver fatty change [MedDRA:10019708]
Liver fatty degeneration [MedDRA:10019708]
Liver fatty deposit [MedDRA:10019708]
Liver fatty deposition [MedDRA:10019708]
Liver fatty infiltration [MedDRA:10019708]
Liver fatty metamorphosis [MedDRA:10019708]
Liver fatty phanerosis [MedDRA:10019708]
Metamorphosis fatty liver [MedDRA:10019708]
Microvesicular fat disease of liver [MedDRA:10019708]
Phanerosis fatty liver [MedDRA:10019708]
Steatosis hepatic [MedDRA:10019708]
Non-alcoholic steatohepatitis [MedDRA:10053219]
Non-alcoholic fatty liver [MedDRA:10053219]
Fatty liver degeneration [OMIM:Fatty liver degeneration]
Steatosis (22%) [OMIM:Steatosis (22%)]
Quality:
Cross references:
Orphanet:29540 "Liver/hepatic steatosis" [Orphanet:29540]
OMIM: "Fatty infiltration of liver" [OMIM:Fatty infiltration of liver]
OMIM: "Fatty liver" [OMIM:Fatty liver]
OMIM: "Hepatic steatosis" [OMIM:Hepatic steatosis]
OMIM: "Liver steatosis" [OMIM:Liver steatosis]
OMIM: "Steatosis" [OMIM:Steatosis]
OMIM: "Fatty liver degeneration" [OMIM:Fatty liver degeneration]
OMIM: "Steatosis (22%)" [OMIM:Steatosis (22%)]
UMLS:C0015695 "Fatty Liver" [Orphanet:29540]
UMLS:C0400966 "Non-alcoholic Fatty Liver Disease" [Orphanet:29540]
UMLS:C2711227 "Steatohepatitis" [Orphanet:29540]
Is a (Direct Parents):
HPO         Abnormality of the liver
Orphanet Decreased liver function
MedDRA Lipid metabolism and deposit disorders NEC
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)
                Hepatic steatosis(HPO:0001397)
MedDRA:
Metabolism and nutrition disorders(MedDRA:10027433)
    Abnormality of lipid metabolism(HPO:0003119)
       Lipid metabolism and deposit disorders NEC(MedDRA:10024581)
          Hepatic steatosis(HPO:0001397)
Congenital, familial and genetic disorders(MedDRA:10010331)
    Metabolic and nutritional disorders congenital(MedDRA:10027424)
       Abnormality of lipid metabolism(HPO:0003119)
          Lipid metabolism and deposit disorders NEC(MedDRA:10024581)
             Hepatic steatosis(HPO:0001397)
Database Frequency: 75 / 7739
Resource:

All diseases associated with this symptom:

19p13.12 microdeletion syndrome (Orphanet:254346)
1p36 deletion syndrome (Orphanet:1606)
3-@HYDROXYACYL-CoA DEHYDROGENASE DEFICIENCY (OMIM:231530)
ARIMA SYNDROME (OMIM:243910)
Acute infantile liver failure-multisystemic involvement syndrome (Orphanet:370088)
Adrenomyodystrophy (Orphanet:977)
Alström syndrome (Orphanet:64)
Bardet-Biedl syndrome 1 (OMIM:209900 )
Bardet-Biedl syndrome 12 (OMIM:615989)
Bardet-Biedl syndrome 16 (OMIM:615993)
Bardet-Biedl syndrome 19 (OMIM:615996)
Bardet-Biedl syndrome 2 (OMIM:615981)
Bardet-Biedl syndrome 5 (OMIM:615983)
Bardet-Biedl syndrome 7 (OMIM:615984)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Bifunctional enzyme deficiency (Orphanet:300)
CARDIOENCEPHALOMYOPATHY, FATAL INFANTILE, DUE TO CYTOCHROME c OXIDASEDEFICIENCY 2 (OMIM:615119)
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 19 (OMIM:615595)
COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 21 (OMIM:615918)
Carnitine palmitoyl transferase 1A deficiency (Orphanet:156)
Carnitine uptake deficiency (Orphanet:158)
Citrullinemia type II (Orphanet:247585)
Classical homocystinuria (Orphanet:394)
Combined oxidative phosphorylation defect type 8 (Orphanet:319504)
Crimean-Congo hemorrhagic fever (Orphanet:99827)
Dorfman-Chanarin disease (Orphanet:98907)
FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1 (OMIM:613282)
FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2 (OMIM:613387)
Familial partial lipodystrophy associated with PLIN1 mutations (Orphanet:280356)
Familial partial lipodystrophy associated with PPARG mutations (Orphanet:79083)
Familial partial lipodystrophy due to AKT2 mutations (Orphanet:79085)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Familial partial lipodystrophy, Köbberling type (Orphanet:79084)
GRACILE syndrome (Orphanet:53693)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Glycogen storage disease due to glycogen branching enzyme deficiency (Orphanet:367)
Hemochromatosis type 3 (Orphanet:225123)
Hemochromatosis type 4 (Orphanet:139491)
Hepatoencephalopathy due to combined oxidative phosphorylation deficiency type 1 (Orphanet:137681)
Hereditary fructose intolerance (Orphanet:469)
Histiocytoid cardiomyopathy (Orphanet:137675)
Hyperinsulinism due to 3-hydroxylacyl-CoA dehydrogenase deficiency (Orphanet:71212)
Hypermethioninemia encephalopathy due to adenosine kinase deficiency (Orphanet:289290)
INFANTILE LIVER FAILURE SYNDROME 2 (OMIM:615486)
Infantile hypertrophic cardiomyopathy due to MRPL44 deficiency (Orphanet:352563)
Infantile regressive hypertriglyceridemia and hepatosteatosis (Orphanet:300293)
Joubert syndrome with oculorenal defect (Orphanet:2318)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 (OMIM:608594)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 (OMIM:269700)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3 (OMIM:612526)
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5 (OMIM:615238)
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 6 (OMIM:615980)
Leigh syndrome (Orphanet:506)
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (Orphanet:5)
MERRF (Orphanet:551)
MORBID OBESITY AND SPERMATOGENIC FAILURE (OMIM:615703)
Mandibular hypoplasia-deafness-progeroid syndrome (Orphanet:363649)
Medium chain acyl-CoA dehydrogenase deficiency (Orphanet:42)
Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency (Orphanet:279934)
Multiple acyl-CoA dehydrogenase deficiency (Orphanet:26791)
Navajo neurohepatopathy (Orphanet:255229)
Neonatal hemochromatosis (Orphanet:446)
Neutral lipid storage myopathy (Orphanet:98908)
PATENT DUCTUS VENOSUS (OMIM:601466)
PMM2-CDG (Orphanet:79318)
Partial acquired lipodystrophy (Orphanet:79087)
Pearson syndrome (Orphanet:699)
Phosphoenolpyruvate carboxykinase 1 deficiency (Orphanet:79316)
Phosphoenolpyruvate carboxykinase 2 deficiency (Orphanet:79317)
Phosphoenolpyruvate carboxykinase deficiency (Orphanet:2880)
Porphyria cutanea tarda (Orphanet:101330)
Primary lipodystrophy (Orphanet:90970)
Renal cysts and diabetes syndrome (Orphanet:93111)
VISCERAL STEATOSIS, CONGENITAL (OMIM:228100)
Very long chain acyl-CoA dehydrogenase deficiency (Orphanet:26793)