Autosomal recessive hereditary disorder
Disorder of fatty acid metabolism
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Fatty acid oxidation defect (disorder)
Fatty acid oxidation defect
Fatty acid oxidation disorder
FAOD - fatty acid oxidation defect
stoornis van vetzuuroxidatie
vetzuuroxidatiestoornis
vetzuuroxidatiedefect
Id1156591005
StatusPrimitive
OccurrenceCongenital
ICD-10 complex map reference set
TargetE71.3
RuleTRUE
AdviceALWAYS E71.3
CorrelationSNOMED CT source code to target map code correlation not specified
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Acyl-CoA dehydrogenase deficiency6
Carnitine acylcarnitine translocase deficiency
Carnitine palmitoyltransferase I deficiency
Carnitine palmitoyltransferase II deficiency3
Deficiency of 3-hydroxyacyl-CoA dehydrogenase
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
Mitochondrial trifunctional protein deficiency4
Renal carnitine transport defect