| Answer | In range | LA18592-8 |
| Answer | Borderline | LA4259-3 |
| Answer | Indeterminate | LA11884-6 |
| Answer | Out of range | LA18593-6 |
| Answer | Out of range requiring further dried blood spot testing for at least one condition | LA12430-7 |
| Answer | Out of range requiring immediate referral | LA25817-0 |
| Answer | Out of range requiring immediate second-tier testing for at least one condition | LA12431-5 |
| Answer | Out of range requiring deferred follow-up for at least one condition | LA18594-4 |
| Answer | One or more tests pending | LA16204-2 |
| Answer | Specimen unsatisfactory for at least one condition | LA16205-9 |
| answers-for | Amino acidemias newborn screen interpretation | 46733-2 |
| answers-for | Fatty acid oxidation defects newborn screen interpretation | 46736-5 |
| answers-for | Galactosemias newborn screen interpretation | 46737-3 |
| answers-for | Hemoglobin disorders newborn screen interpretation | 46740-7 |
| answers-for | Maple syrup urine disease newborn screen interpretation | 46743-1 |
| answers-for | Organic acidemias newborn screen interpretation | 46744-9 |
| answers-for | Phenylketonuria and variants/Biopterin defects newborn screen interpretation | 46746-4 |
| answers-for | Congenital adrenal hyperplasia newborn screen interpretation | 46758-9 |
| answers-for | Biotinidase deficiency newborn screen interpretation | 46761-3 |
| answers-for | Congenital hypothyroidism newborn screen interpretation | 46762-1 |
| answers-for | Cystic fibrosis newborn screen interpretation | 46769-6 |
| answers-for | Acylcarnitine newborn screen interpretation | 58088-6 |
| answers-for | Glucose-6-Phosphate dehydrogenase newborn screen interpretation | 58089-4 |
| answers-for | Lysosomal storage disorders newborn screen interpretation | 62301-7 |
| answers-for | Fabry disease newborn screen interpretation | 62305-8 |
| answers-for | Krabbe disease newborn screen interpretation | 62308-2 |
| answers-for | Gaucher disease newborn screen interpretation | 62312-4 |
| answers-for | Niemann Pick disease A/B newborn screen interpretation | 62318-1 |
| answers-for | Severe combined immunodeficiency newborn screen interpretation | 62321-5 |
| answers-for | Pompe disease newborn screen interpretation | 63415-4 |
| answers-for | Multiple carboxylase deficiency (MCD) newborn screen interpretation | 73701-5 |
| answers-for | Mucopolysaccharidosis type I newborn screen interpretation | 79564-1 |
| answers-for | X-linked adrenoleukodystrophy newborn screen interpretation | 85269-9 |
| answers-for | Spinal muscular atrophy newborn screen interpretation | 92004-1 |
| LONG_COMMON_NAME | en-US | NBS interp |
LOINC Version: 2.77
FHIR