Fatty acid oxidation defects   LP56738-5

LOINC Hierarchy


Select the title to see children of the section (▸) or the LOINC code. Select a code to view information about the section/code.

Carnitine uptake defect/CPT1 deficiency   LP56763-3

Fatty acid oxidation defects | DBS | Chemistry - non-challenge   LP385866-1

CPT2/CACT   LP57638-6

Fatty acid oxidation   LP33265-7

Fatty acid oxidation conditions suspected   LP97724-6

Long Chain Hydroxy Acyl Dehydrogenase/Trifunctional Protein Deficiencies   LP56761-7

Medium chain acyl dehydrogenase Deficiency/Glutaric Acidemia type 2   LP56758-3

Medium/Short chain acyl-CoA dehydrogenase deficiency   LP56927-4

Short-chain acyl-CoA deficiency (SCAD); ethylmalonic encephalopathy; isobutyryl-CoA dehydrogenase deficiency   LP56792-2

Short-chain acyl-CoA dehydrogenase deficiency   LP174562-1

Very long chain hydroxy acyl dehydrogenase deficiency   LP56760-9

Other fatty acid oxidation disorders   LP56765-8

Fatty acid oxidation defects newborn screening comment/discussion   LP97615-6


Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2024, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.

demo
request yours today
subscribe
start today
newsletter
free subscription

Thank you for choosing Find-A-Code, please Sign In to remove ads.