700463002: Alpha-methylacyl-CoA racemase deficiency disorder (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Viscus structure finding\Abdominal organ finding\Liver finding\Disorder of liver\Metabolic and genetic disorder affecting the liver\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder
• \Digestive system finding\Liver finding\Disorder of liver\Metabolic and genetic disorder affecting the liver\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder
• \Digestive system finding\Disorder of digestive system\Digestive system hereditary disorder\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder
• \Digestive system finding\Disorder of digestive system\Disorder of digestive organ\Disorder of liver\Metabolic and genetic disorder affecting the liver\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\Metabolic and genetic disorder affecting the liver\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Abdominal organ finding\Liver finding\Disorder of liver\Metabolic and genetic disorder affecting the liver\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder
• \Finding of trunk structure\Finding of abdominopelvic segment of trunk\Finding of abdomen\Disorder of abdomen\Disorder of liver\Metabolic and genetic disorder affecting the liver\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder
• \Finding of trunk structure\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\Metabolic and genetic disorder affecting the liver\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\General loss of peroxisomal function\Alpha-methylacyl-CoA racemase deficiency disorder
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Digestive system hereditary disorder\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Alpha-methylacyl-CoA racemase deficiency disorder
• \Disease\Disorder of body system\Hereditary disorder by system\Digestive system hereditary disorder\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder
• \Disease\Disorder of body system\Disorder of digestive system\Digestive system hereditary disorder\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder
• \Disease\Disorder of body system\Disorder of digestive system\Disorder of digestive organ\Disorder of liver\Metabolic and genetic disorder affecting the liver\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder
• \Disease\Disorder of trunk\Disorder of abdominopelvic segment of trunk\Disorder of abdomen\Disorder of liver\Metabolic and genetic disorder affecting the liver\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Disorder of peroxisomal function\General loss of peroxisomal function\Alpha-methylacyl-CoA racemase deficiency disorder
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder
• \Disease\Metabolic disease\Metabolic and genetic disorder affecting the liver\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder
• \Disease\Metabolic disease\Disorder of lipoprotein AND/OR lipid metabolism\Disorder of lipid metabolism\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder
• \Disease\Congenital disease\Inborn error of metabolism\Disorder of peroxisomal function\General loss of peroxisomal function\Alpha-methylacyl-CoA racemase deficiency disorder
• \Disease\Congenital disease\Inborn error of metabolism\Synthetic defect of bile acids\Alpha-methylacyl-CoA racemase deficiency disorder

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2014. Module: SNOMED CT core module

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
2990662014	Alpha-methylacyl-CoA racemase deficiency disorder	en	Synonym	Active	Only initial character case insensitive	SNOMED CT core module
2990699014	Alpha-methylacyl-CoA racemase deficiency disorder (disorder)	en	Fully specified name	Active	Only initial character case insensitive	SNOMED CT core module
2990734011	AMACR deficiency	en	Synonym	Active	Entire term case sensitive	SNOMED CT core module
4570900017	Congenital bile acid synthesis defect type 4	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module

Expanded Value Set

This concept is not in any reference sets

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