71592-0

Hemoglobinopathies conditions suspected [Identifier] in DBS

Active

Fully-Specified Name

Component: Hemoglobinopathies conditions suspected
Property: Prid
Time: Pt
System: Bld.dot
Scale: Nom
Method

Additional Names

Short Name: Hemoglobinopathies suspected DBS
Display Name: Hemoglobinopathies conditions suspected Nom (DBS)
Consumer Name Alpha Get Info: Hemoglobinopathies conditions suspected, Dried blood spot

Example Answer List: LL2094-2

Source: National Institutes of Health

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

Basic Attributes

Class: CHEM
Type: Laboratory
First Released: Version 2.40
Last Updated: Version 2.61
Change Reason: Changed answer list from "Normative" to "Example" to fit the current LOINC model.
Order vs. Observation: Observation

Member of these Panels

LOINC	Long Common Name
104191-2	Guanidinoacetate methyltransferase (GAMT) deficiency newborn screening panel
54081-5	Hemoglobinopathies newborn screening panel
54089-8	Newborn screening panel American Health Information Community (AHIC)

Language Variants Get Info

Tag	Language	Translation
es-ES	Spanish (Spain)	Condiciones de susceptibilidad de hemoglobinopatías:Presencia o identidad:Punto temporal:gota de sangre (papel de filtro):Nom:
es-MX	Spanish (Mexico)	Sospecha de condiciones de hemoglobinopatías:Presencia o identidad:Punto temporal:DBS:Nominal:
fr-FR	French (France)	Hémoglobinopathies conditions suspectées:Identification:Ponctuel:Sang buvard:Résultat nominal:
it-IT	Italian (Italy)	Emoglobinopatie, condizioni sospette:Prid:Pt:Sangue.su carta da filtro:Nom: Synonyms: Chimica Presenza o Identità Punto nel tempo (episodio) Sangue Spot sangue secco
nl-NL	Dutch (Netherlands)	hemoglobinopathie-aandoeningen vermoed:identificator:moment:gedroogde bloedspot:nominaal: Synonyms: hemoglobinopathie aandoeningen vermoed
pl-PL	Polish (Poland)	Podejrzenie hemoglobinopatii:wykrycie lub identyfikacja:punkt w czasie:sucha kropla krwi:cecha:
pt-BR	Portuguese (Brazil)	Hemoglobinopatias condições suspeitas:Ident:Pt:SgPapel:Nom:
ru-RU	Russian (Russian Federation)	Гемоглобинопатии состояние заподозренное:ПрИд:ТчкВрм:Кр.Сух.капл:Ном: Synonyms: Кровь Кровь сухая капля Номинальный;Именной Подозрение на гемоглобинопатии Присутствие или Идентификация Точка во времени;Момент
tr-TR	Turkish (Turkey)	Hemoglobinopati durumları süphelenilen:MevcKimlik:Zmlı:Kan.nokta:Snf:
zh-CN	Chinese (China)	所怀疑的血红蛋白病:存在与否或特征标识:时间点:全血.斑点:名义型: Synonyms: 全血斑点(滤纸);滤纸;血液.斑点;血液斑点(滤纸) 分类型应答;分类型结果;名义性;名称型;名词型;名词性;标称性;没有自然次序的名义型或分类型应答化学;化学检验项目;化学检验项目类;化学类;化学试验;非刺激耐受型化学检验项目;非刺激耐受型化学检验项目类;非刺激耐受型化学试验;非刺激耐受型化学试验类存在;存在与否;特征标识;身份;身份标识所怀疑的血红蛋白病类型;所怀疑的血红蛋白病情况;疑似血红蛋白病时刻;随机;随意;瞬间血;血液

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