LL6931-1
NBS new
Active
Basic Properties
- OID
- 1.3.6.1.4.1.12009.10.1.5748
- Name
- NBS new
- Description
- Answers: ?; Scale: ?; Code: ?; Score: ?
- LOINCs using this list
- 26
Answer List
| Answer | Code | Score | Answer ID |
|---|---|---|---|
| Borderline | LA4259-3 | ||
| IndeterminateCopyright http://snomed.info/sct ID:82334004 Indeterminate (qualifier value) | LA11884-6 | ||
| One or more tests pending | LA16204-2 | ||
| Screen Negative | LA34518-3 | ||
| Screen Positive | LA34519-1 | ||
| Specimen unacceptable for at least one condition | LA34520-9 | ||
| InconclusiveCopyright http://snomed.info/sct ID:419984006 Inconclusive (qualifier value) | LA9663-1 | ||
| Not tested | LA13538-6 |
LOINC terms using this Answer List
| 58088-6 | Acylcarnitine newborn screen interpretation |
| 46733-2 | Amino acidemias newborn screen interpretation |
| 46761-3 | Biotinidase deficiency newborn screen interpretation |
| 46758-9 | Congenital adrenal hyperplasia newborn screen interpretation |
| 46762-1 | Congenital hypothyroidism newborn screen interpretation |
| 46769-6 | Cystic fibrosis newborn screen interpretation |
| 62305-8 | Fabry disease newborn screen interpretation |
| 46736-5 | Fatty acid oxidation defects newborn screen interpretation |
| 46737-3 | Galactosemias newborn screen interpretation |
| 62312-4 | Gaucher disease newborn screen interpretation |
| 58089-4 | Glucose-6-Phosphate dehydrogenase newborn screen interpretation |
| 104192-0 | Guanidinoacetate methyltransferase deficiency newborn screen interpretation |
| 46740-7 | Hemoglobin disorders newborn screen interpretation |
| 62308-2 | Krabbe disease newborn screen interpretation |
| 62301-7 | Lysosomal storage disorders newborn screen interpretation |
| 46743-1 | Maple syrup urine disease newborn screen interpretation |
| 79564-1 | Mucopolysaccharidosis type I newborn screen interpretation |
| 104189-6 | Mucopolysaccharidosis type II newborn screen interpretation newborn screen interpretation |
| 73701-5 | Multiple carboxylase deficiency (MCD) newborn screen interpretation |
| 62318-1 | Niemann Pick disease A/B newborn screen interpretation |
| 46744-9 | Organic acidemias newborn screen interpretation |
| 46746-4 | Phenylketonuria and variants/Biopterin defects newborn screen interpretation |
| 63415-4 | Pompe disease newborn screen interpretation |
| 62321-5 | Severe combined immunodeficiency newborn screen interpretation |
| 92004-1 | Spinal muscular atrophy newborn screen interpretation |
| 85269-9 | X-linked adrenoleukodystrophy newborn screen interpretation |
LOINC Terminology Service (API) using HL7® FHIR® Get Info
Requests to this service require a free LOINC username and password. Below is a sample of the possible capabilities. See the LOINC Terminology Service documentation for more information.
- CodeSystem lookup
- https:
//fhir.loinc.org/CodeSystem/$lookup?system=http: //loinc.org&code=LL6931-1 - ValueSet definition
- https:
//fhir.loinc.org/ValueSet/?url=http: //loinc.org/vs/LL6931-1 - ValueSet expansion
- https:
//fhir.loinc.org/ValueSet/$expand?url=http: //loinc.org/vs/LL6931-1
Third Party Copyright
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LOINC Copyright
Copyright © Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://