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1156591005: Fatty acid oxidation defect (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4575323013 Fatty acid oxidation defect (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
4575324019 Fatty acid oxidation defect en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4575325018 Fatty acid oxidation disorder en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4575326017 FAOD - fatty acid oxidation defect en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core


21 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Fatty acid oxidation defect (disorder) est un(e) (attribut) Autosomal recessive hereditary disorder true Inferred relationship Some
Fatty acid oxidation defect (disorder) survenue (attribut) congénital true Inferred relationship Some 1
Fatty acid oxidation defect (disorder) est un(e) (attribut) Disorder of fatty acid metabolism true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group
Acyl-CoA dehydrogenase deficiency est un(e) (attribut) True Fatty acid oxidation defect (disorder) Inferred relationship Some
Renal carnitine transport defect est un(e) (attribut) True Fatty acid oxidation defect (disorder) Inferred relationship Some
Deficiency of 3-hydroxyacyl-CoA dehydrogenase est un(e) (attribut) True Fatty acid oxidation defect (disorder) Inferred relationship Some
Mitochondrial trifunctional protein deficiency est un(e) (attribut) True Fatty acid oxidation defect (disorder) Inferred relationship Some
Carnitine palmitoyltransferase I deficiency est un(e) (attribut) True Fatty acid oxidation defect (disorder) Inferred relationship Some
Carnitine palmitoyltransferase II deficiency est un(e) (attribut) True Fatty acid oxidation defect (disorder) Inferred relationship Some
Carnitine acylcarnitine translocase deficiency est un(e) (attribut) True Fatty acid oxidation defect (disorder) Inferred relationship Some
Long chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (disorder) est un(e) (attribut) True Fatty acid oxidation defect (disorder) Inferred relationship Some
Autosomal recessive glutaric aciduria, type 2 est un(e) (attribut) False Fatty acid oxidation defect (disorder) Inferred relationship Some

This concept is not in any reference sets

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