FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 4.0.1  |  FHIR Version n/a  User: [n/a]

39929009: Disorder of fatty acid metabolism (disorder)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
492317010 Disorders of fatty-acid metabolism en Synonym Active Case insensitive SNOMED CT core
492318017 Disorder of fat oxidation en Synonym Active Case insensitive SNOMED CT core
66517017 Disorder of fatty acid metabolism en Synonym Active Case insensitive SNOMED CT core
66518010 Disorder of fatty acid metabolism, NOS en Synonym Inactive Initial character case insensitive SNOMED CT core
776475011 Disorder of fatty acid metabolism (disorder) en Fully specified name Active Case insensitive SNOMED CT core

38 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Disorder of fatty acid metabolism Is a Disorder of lipoprotein AND/OR lipid metabolism true Inferred relationship Some
Disorder of fatty acid metabolism Is a Inborn error of metabolism true Inferred relationship Some
Disorder of fatty acid metabolism Is a Organic acid metabolism disorder true Inferred relationship Some
Disorder of fatty acid metabolism Occurrence Congenital true Inferred relationship Some 1
Disorder of fatty acid metabolism Finding site Body system structure false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Fatty acid oxidation defect Is a True Disorder of fatty acid metabolism Inferred relationship Some
Combined malonic and methylmalonic aciduria Is a True Disorder of fatty acid metabolism Inferred relationship Some
Deficiency of butyryl-CoA dehydrogenase Is a False Disorder of fatty acid metabolism Inferred relationship Some
Deficiency of acyl-CoA dehydrogenase Is a False Disorder of fatty acid metabolism Inferred relationship Some
Malonic aciduria Is a True Disorder of fatty acid metabolism Inferred relationship Some
Malonyl-CoA decarboxylase deficiency Is a False Disorder of fatty acid metabolism Inferred relationship Some
Renal carnitine transport defect Is a False Disorder of fatty acid metabolism Inferred relationship Some
Glutaric aciduria, type 2 Is a True Disorder of fatty acid metabolism Inferred relationship Some
Phytanic acid storage disease Is a True Disorder of fatty acid metabolism Inferred relationship Some
Deficiency of malonyl-CoA decarboxylase Is a False Disorder of fatty acid metabolism Inferred relationship Some
Carnitine acetyltransferase deficiency Is a False Disorder of fatty acid metabolism Inferred relationship Some
Iatrogenic carnitine deficiency Is a False Disorder of fatty acid metabolism Inferred relationship Some
Acyl-CoA dehydrogenase deficiency Is a False Disorder of fatty acid metabolism Inferred relationship Some
Muscle carnitine deficiency Is a False Disorder of fatty acid metabolism Inferred relationship Some
Carnitine palmitoyltransferase deficiency Is a True Disorder of fatty acid metabolism Inferred relationship Some
Long-chain fatty acid transport deficiency Is a True Disorder of fatty acid metabolism Inferred relationship Some
Deficiency of carnitine acetyltransferase Is a True Disorder of fatty acid metabolism Inferred relationship Some
Deficiency of 2,4-dienoyl-CoA reductase Is a True Disorder of fatty acid metabolism Inferred relationship Some
Mitochondrial trifunctional protein deficiency Is a False Disorder of fatty acid metabolism Inferred relationship Some
Combined deficiency of long chain 3-hydroxyacyl-CoA dehydrogenase and enoyl-CoA hydratase Is a True Disorder of fatty acid metabolism Inferred relationship Some
Carnitine acylcarnitine translocase deficiency Is a False Disorder of fatty acid metabolism Inferred relationship Some
Succinyl-CoA acetoacetate transferase deficiency Is a True Disorder of fatty acid metabolism Inferred relationship Some
Carnitine deficiency due to inborn error of metabolism Is a True Disorder of fatty acid metabolism Inferred relationship Some
HMG-CoA synthase deficiency Is a True Disorder of fatty acid metabolism Inferred relationship Some
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency Is a False Disorder of fatty acid metabolism Inferred relationship Some

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Back to Start