OMOP Concept 4342777
Metabolic and genetic disorder affecting the liver
StandardConditionSNOMED235903001Disorder
Maps from
1
Descendants
44
Valid from
31 Jan 2002
Valid to
31 Dec 2099
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Source codes that map to this concept
1 source code normalizes to Metabolic and genetic disorder affecting the liver via the OMOP "Maps to" relationship.
| Vocabulary | Code | Name | Type |
|---|---|---|---|
| Nebraska Lexicon | 235903001 | Metabolic and genetic disorder affecting the liver | Non-standard |
Synonyms
Alternative names recorded for Metabolic and genetic disorder affecting the liver across source vocabularies.
- Metabolic and genetic disorder affecting the liver (disorder)
- trastorno metabólico y genético que afecta el hígado
- trastorno metabólico y genético que afecta el hígado (trastorno)
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(21)Roll up to these when you need a wider cohort.
- 1Disease of liver
- 1Metabolic disease
- 2Disease
- 2Disorder of liver and/or biliary tract
- 2Liver finding
- 2OMOP Acute Liver Failure 1
- 2OMOP Acute Liver Failure 2
- 2OMOP Acute Liver Failure 8
- 3Abdominal organ finding
- 3Clinical finding
- 3Digestive system finding
- 3Disorder of abdomen
- 3Disorder of digestive organ
- 4Disorder of abdominopelvic segment of trunk
- 4Disorder of digestive system
- 4Finding of abdomen
- 4Viscus structure finding
- 5Disorder of body system
- 5Disorder of trunk
- 5Finding of abdominopelvic segment of trunk
- 6Finding of trunk structure
Narrower concepts
(44)Included automatically when you query with descendants.
- 1Alpha-1-antitrypsin deficiency
- 1Antichymotrypsin deficiency-alpha-1
- 1Congenital cystic disease of liver
- 1Contiguous ABCD1 DXS1357E deletion syndrome
- 1Digenic hemochromatosis
- 1Dubin-Johnson syndrome
- 1Ferro-cerebro-cutaneous syndrome
- 1FTH1-related iron overload
- 1Glycogen storage disease, hepatic form
- 1Hepatoencephalopathy due to combined oxidative phosphorylation defect type 1
- 1Liver calculus
- 1Mitochondrial DNA depletion syndrome, hepatocerebral form due to DGUOK deficiency
- 1Mitochondrial DNA depletion syndrome hepatocerebrorenal form
- 1Mucopolysaccharidosis, MPS-II
- 1Navajo neurohepatopathy
- 1Primary copper-associated hepatitis
- 1Progressive intrahepatic cholestasis
- 1Steroid dehydrogenase deficiency and dental anomaly syndrome
- 1Synthetic defect of bile acids
- 1Wilson's disease
- 23-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency
- 2Alpha-methylacyl-CoA racemase deficiency disorder
- 2Bile acid CoA ligase deficiency and defective amidation
- 2Cholestanol storage disease
- 2Chorea co-occurrent and due to Wilson disease
- 2Congenital bile acid synthesis defect type 3
- 2Delta-4-3-oxosteroid-5-beta-reductase deficiency
- 2Familial hypercholanemia
- 2Glycogen storage disease, type I
- 2Glycogen storage disease type III
- 2Glycogen storage disease, type IV
- 2Glycogen storage disease, type VI
- 2Glycogen storage disease type VIII
- 2Hunter's syndrome, mild form
- 2Hunter's syndrome, severe form
- 2Hypercholesterolemia due to cholesterol 7alpha-hydroxylase deficiency
- 2North American Indian childhood cirrhosis
- 2Progressive familial intrahepatic cholestasis type 1
- 2Progressive familial intrahepatic cholestasis type 2
- 2Progressive familial intrahepatic cholestasis type 3
- 2Progressive familial intrahepatic cholestasis type 4
- 2Westphal-Strumpell syndrome
- 3Glucose-6-phosphate transport defect
- 3Glycogen storage disease type Ia
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