LL2094-2
NBS Hb
Active
Basic Properties
- OID
- 1.3.6.1.4.1.12009.10.1.1249
- Name
- NBS Hb
- Description
- Newborn Screenin Hemoglobinopathies
- LOINCs using this list
- 1
Answer List
| Answer | Code | Score | Answer ID |
|---|---|---|---|
| NoneCopyright http://snomed.info/sct ID:260413007 None (qualifier value) Screen time |
LA137-2 | ||
| Likely transfusionCopyright http://snomed.info/sct ID:10593005 Posttransfusion state (finding) | LA18557-1 | ||
| Hb SS-disease (sickle cell anemia)Copyright http://snomed.info/sct ID:127040003 Sickle cell-hemoglobin SS disease (disorder) | LA12614-6 | ||
| Hb S (sickle)-carrierCopyright http://snomed.info/sct ID:16402000 Sickle cell trait (disorder) | LA12606-2 | ||
| Hb S beta plus thalassemiaCopyright http://snomed.info/sct ID:127042006 Sickle cell beta plus thalassemia (disorder) | LA18558-9 | ||
| Hb S beta zero thalassemiaCopyright http://snomed.info/sct ID:127043001 Sickle cell-beta^0^-thalassemia (disorder) | LA18559-7 | ||
| Hb S beta-thalassemiaCopyright http://snomed.info/sct ID:127041004 Sickle cell-beta-thalassemia (disorder) | LA12615-3 | ||
| Hb SC-diseaseCopyright http://snomed.info/sct ID:35434009 Sickle cell-hemoglobin C disease (disorder) | LA12616-1 | ||
| Hb SD-diseaseCopyright http://snomed.info/sct ID:25472008 Sickle cell-hemoglobin D disease (disorder) | LA12617-9 | ||
| Hb SE-diseaseCopyright http://snomed.info/sct ID:47024008 Sickle cell-hemoglobin E disease (disorder) | LA12618-7 | ||
| Hb S,O-Arab | LA13012-2 | ||
| Hb S variant | LA18560-5 | ||
| Hb S/Hereditary persistence of fetal hemoglobinCopyright http://snomed.info/sct ID:234391009 Sickle cell anemia with high hemoglobin F (disorder) | LA18561-3 | ||
| Homozygous Hereditary persistence of fetal hemoglobinCopyright http://snomed.info/sct ID:191201002 Hereditary persistence of fetal hemoglobin (disorder) | LA18562-1 | ||
| Beta plus thalassemiaCopyright http://snomed.info/sct ID:79592006 Beta plus thalassemia (disorder) | LA18563-9 | ||
| Hb beta zero-thalassemiaCopyright http://snomed.info/sct ID:86715000 Beta zero thalassemia (disorder) | LA12611-2 | ||
| Beta thalassemiaCopyright http://snomed.info/sct ID:65959000 beta Thalassemia (disorder) | LA18564-7 | ||
| Hb C-diseaseCopyright http://snomed.info/sct ID:51053007 Hemoglobin C disease (disorder) | LA12607-0 | ||
| Hb C-carrierCopyright http://snomed.info/sct ID:76050008 Hemoglobin C trait (disorder) | LA12602-1 | ||
| Hb C beta plus thalassemiaCopyright http://snomed.info/sct ID:119691000119106 Hemoglobin C/beta thalassemia disease (disorder) | LA18565-4 | ||
| Hb C beta zero thalassemiaCopyright http://snomed.info/sct ID:119691000119106 Hemoglobin C/beta thalassemia disease (disorder) | LA18566-2 | ||
| Hb C beta-thalassemiaCopyright http://snomed.info/sct ID:119691000119106 Hemoglobin C/beta thalassemia disease (disorder) | LA12608-8 | ||
| Hb Constant Spring carrier | LA19957-2 | ||
| Hb D-disease | LA12609-6 | ||
| Hb D-carrierCopyright http://snomed.info/sct ID:7391009 Hemoglobin D trait (disorder) | LA12603-9 | ||
| Hb D beta plus thalassemia | LA18567-0 | ||
| Hb D beta zero thalassemia | LA18568-8 | ||
| Hb D beta-thalassemiaCopyright http://snomed.info/sct ID:119701000119106 Hemoglobin D/beta thalassemia disease (disorder) | LA12610-4 | ||
| Hb E-diseaseCopyright http://snomed.info/sct ID:25065001 Hemoglobin E disease (disorder) | LA12612-0 | ||
| Hb E-carrierCopyright http://snomed.info/sct ID:46248003 Hemoglobin E trait (disorder) | LA12604-7 | ||
| Hb E beta plus thalassemiaCopyright http://snomed.info/sct ID:234392002 Hemoglobin E/beta thalassemia disease (disorder) | LA18569-6 | ||
| Hb E beta zero thalassemiaCopyright http://snomed.info/sct ID:234392002 Hemoglobin E/beta thalassemia disease (disorder) | LA18570-4 | ||
| Hb E delta beta thalassemiaCopyright http://snomed.info/sct ID:234392002 Hemoglobin E/beta thalassemia disease (disorder) | LA18571-2 | ||
| Hb E beta-thalassemiaCopyright http://snomed.info/sct ID:234392002 Hemoglobin E/beta thalassemia disease (disorder) | LA12613-8 | ||
| Hb G disease | LA18572-0 | ||
| Hb G carrier | LA18573-8 | ||
| Hb G beta plus thalassemia | LA18574-6 | ||
| Hb G beta thalassemia | LA18575-3 | ||
| Hb G beta zero thalassemia | LA18576-1 | ||
| Hb D/G disease | LA18577-9 | ||
| Hb D/G carrier | LA18578-7 | ||
| Hb D/G beta plus thalassemia | LA18579-5 | ||
| Hb D/G beta thalassemia | LA18580-3 | ||
| Hb D/G beta zero thalassemia | LA18581-1 | ||
| Hb O-Arab carrier | LA12605-4 | ||
| Alpha thalassemia majorCopyright http://snomed.info/sct ID:5300004 Hemoglobin Bart's hydrops syndrome (disorder) | LA18582-9 | ||
| Alpha thalassemia traitCopyright http://snomed.info/sct ID:191187006 Alpha trait thalassemia (disorder) | LA18583-7 | ||
| Hb H diseaseCopyright http://snomed.info/sct ID:48553001 Hemoglobin H disease (disorder) | LA18584-5 | ||
| Hb H Constant Spring diseaseCopyright http://snomed.info/sct ID:447117006 Hemoglobin H constant spring thalassemia (disorder) | LA18585-2 | ||
| Hb H with other variant point mutations | LA18586-0 | ||
| Other Hb diseaseCopyright http://snomed.info/sct ID:123772008 Homozygous hemoglobinopathy (disorder) | LA18587-8 | ||
| Other Hb carrier | LA18588-6 | ||
| Other beta plus thalassemia | LA18589-4 | ||
| Other beta zero thalassemia | LA18590-2 | ||
| Other beta thalassemia | LA18591-0 |
LOINC terms using this Answer List
| 71592-0 | Hemoglobinopathies conditions suspected [Identifier] in DBS |
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/$lookup?system=http: //loinc.org&code=LL2094-2 - ValueSet definition
- https:
//fhir.loinc.org/ValueSet/?url=http: //loinc.org/vs/LL2094-2 - ValueSet expansion
- https:
//fhir.loinc.org/ValueSet/$expand?url=http: //loinc.org/vs/LL2094-2
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