| parent | Newborn screening panel | LP33025-5 |
| child | Carnitine uptake defect &or CPT1 deficiency | LP56763-3 |
| child | Fatty acid oxidation defects | DBS | Chemistry - non-challenge | LP385866-1 |
| child | CPT2 &or CACT | LP57638-6 |
| child | Fatty acid oxidation | LP33265-7 |
| child | Fatty acid oxidation conditions suspected | LP97724-6 |
| child | Long chain hydroxy acyl dehydrogenase &or trifunctional protein deficiencies | LP56761-7 |
| child | Medium chain acyl dehydrogenase deficiency &or glutaric acidemia type 2 | LP56758-3 |
| child | Medium &or short chain acyl-CoA dehydrogenase deficiency | LP56927-4 |
| child | Short-chain acyl-CoA deficiency &or ethylmalonic encephalopathy &or isobutyryl-CoA dehydrogenase deficiency | LP56792-2 |
| child | Short-chain acyl-CoA dehydrogenase deficiency | LP174562-1 |
| child | Very long chain hydroxy acyl dehydrogenase deficiency | LP56760-9 |
| child | Other fatty acid oxidation disorders | LP56765-8 |
| child | Fatty acid oxidation defects newborn screening comment-discussion | LP97615-6 |
| PartDisplayName | en-US | Fatty acid oxidation defects |
| DisplayName | en-US | Fatty acid oxidation defects |
LOINC Version: 2.77
FHIR