CPT Changes Current book and archives back to 2000 Easy-to-read online book format Linked to and from code details
learn more
Fatty acid oxidation defect 1156591005 SNOMED CT code SNOMED code 1156591005 name Fatty acid oxidation defect status active date introduced 2021-07-31 fully specified name(s) Fatty acid oxidation defect (disorder) synonyms Fatty acid oxidation defect Fatty acid oxidation disorder FAOD - fatty acid oxidation defect attributes - group1 Occurrence Congenital 255399007 parents Disorder of fatty acid metabolism 39929009 Autosomal recessive hereditary disorder 85995004 children Acyl-CoA dehydrogenase deficiency 82319005 Carnitine acylcarnitine translocase deficiency 238003000 Carnitine palmitoyltransferase I deficiency 238001003 Carnitine palmitoyltransferase II deficiency 238002005 Deficiency of 3-hydroxyacyl-CoA dehydrogenase 124122005 Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency 726021008 Mitochondrial trifunctional protein deficiency 237999008 Renal carnitine transport defect 21764004 hierarchies a selection of possible paths
SNOMED CT Concept 138875005 404684003 64572001 75934005 116021002 39929009 1156591005 138875005 404684003 64572001 782964007 32895009 1899006 85995004 1156591005 ancestors sorted most to least specific
cpt crosswalks Rules-based maps relating CPT® codes to and from SNOMED CT® clinical concepts. Forward and backward mapping allows for easy transition between code sets. Map-A-Code crosswalk tool easily crosswalks multiple codes between the code sets.
Access to this feature is available in the following products:CPT® to SNOMED Crosswalks sign IN sign UP
Thank you for choosing Find-A-Code, please Sign In to remove ads.
Quick, Current, Complete - www.findacode.com