LOINC Home

{component}   LP432695-7

Laboratory   LP29693-6

Chemistry and Chemistry - challenge   LP343631-0

Chemistry - non-challenge   LP7786-9

Newborn screening panel   LP33025-5

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 © 2023 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2023, 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.

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