Hepatic steatosis
Symptom Information:
Symptom ID: | HPO:0001397 | |||||||||||||||||||||||||||||||||||||||||||||||
Synonyms: |
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Cross references: |
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Is a (Direct Parents): |
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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) |
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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) |