57720-5

Newborn conditions with equivocal markers [Identifier] in DBS

Active

Fully-Specified Name

Component: Newborn conditions with equivocal markers
Property: Prid
Time: Pt
System: Bld.dot
Scale: Nom
Method

Additional Names

Short Name: NB conditions with equivocal markers
Display Name: Newborn conditions with equivocal markers Nom (DBS)
Consumer Name Alpha Get Info: Newborn conditions with equivocal markers, Dried blood spot

Preferred Answer List: LL835-0

Source: Regenstrief Institute

Answer	Code	Answer ID
NoneCopyright http://snomed.info/sct ID:260413007 None (qualifier value) Screen time		LA137-2
Hearing lossCopyright http://snomed.info/sct ID:15188001 Hearing loss (disorder)	HEAR	LA24366-9
2-Methyl-3-hydroxybutyric aciduriaCopyright http://snomed.info/sct ID:791000124107 2-methyl-3-hydroxybutyric aciduria (disorder)	2M3HBA	LA12464-6
2-MethylbutyrylglycinuriaCopyright http://snomed.info/sct ID:445596006 2-methylbutyrylglycinuria (disorder)	2MBG	LA12465-3
3-Methylcrotonyl-CoA carboxylase deficiencyCopyright http://snomed.info/sct ID:13144005 Methylcrotonyl-coenzyme A carboxylase deficiency (disorder)	3-MCC	LA12466-1
3-Methylcrotonyl-CoA carboxylase deficiency (maternal)Copyright http://snomed.info/sct ID:206001006 Fetal or neonatal effect of maternal problem unrelated to pregnancy (disorder)	3-MCC (mat)	LA12467-9
3-Methylglutaconic aciduriaCopyright http://snomed.info/sct ID:237950009 3-Methylglutaconic aciduria (disorder)	3MGA	LA12468-7
Pyroglutamic acidemiaCopyright http://snomed.info/sct ID:39112005 Glutathione synthase deficiency with 5-oxoprolinuria (disorder)	5-OXO	LA12469-5
Argininemia	ARG	LA21161-7
Argininosuccinic aciduria	ASA	LA21162-5
Biopterin defect in cofactor biosynthesisCopyright http://snomed.info/sct ID:237914002 6-Pyruvoyl-tetrahydrobiopterin synthase deficiency (disorder)	BIOPT-BS	LA12472-9
Biopterin defect in cofactor regenerationCopyright http://snomed.info/sct ID:58256000 Dihydropteridine reductase deficiency (disorder)	BIOPT-REG	LA12473-7
Beta-ketothiolase deficiencyCopyright http://snomed.info/sct ID:237953006 Mitochondrial 2-methylacetoacetyl-CoA thiolase deficiency - potassium stimulated (disorder)	BKT	LA12474-5
Carnitine acylcarnitine translocase deficiencyCopyright http://snomed.info/sct ID:238003000 Carnitine acylcarnitine translocase deficiency (disorder)	CACT	LA12475-2
Cobalamin A diseaseCopyright http://snomed.info/sct ID:73843004 Cobalamin A disease (disorder)	CBL A	LA12476-0
Cobalamin B diseaseCopyright http://snomed.info/sct ID:82245003 Cobalamin B disease (disorder)	CBL B	LA12477-8
Cobalamin C diseaseCopyright http://snomed.info/sct ID:74653006 Cobalamin C disease (disorder)	CBL C	LA12478-6
Cobalamin D diseaseCopyright http://snomed.info/sct ID:31220004 Cobalamin D disease (disorder)	CBL D	LA12479-4
Cobalamin E diseaseCopyright http://snomed.info/sct ID:360373000 Homocystinuria vitamin B12-responsive type III (disorder)	CBL E	LA12480-2
CBL G type Methylcobalamin deficiencyCopyright http://snomed.info/sct ID:721187005 Methylcobalamin deficiency type cbl G (disorder)	CBL G	LA12481-0
Citrullinemia, type ICopyright http://snomed.info/sct ID:398680004 Citrullinemia (disorder)	CIT-I	LA12482-8
Citrullinemia, type IICopyright http://snomed.info/sct ID:716863007 Citrullinemia type II (disorder)	CIT-II	LA12483-6
Carbamoyl-phosphate synthase deficiencyCopyright http://snomed.info/sct ID:62522004 Congenital hyperammonemia, type I (disorder)	CPS	LA12484-4
Carnitine palmitoyltransferase type I deficiencyCopyright http://snomed.info/sct ID:238001003 Carnitine palmitoyltransferase I deficiency (disorder)	CPT-Ia	LA12485-1
Carnitine palmitoyltransferase type II deficiencyCopyright http://snomed.info/sct ID:238002005 Carnitine palmitoyltransferase II deficiency (disorder)	CPT-II	LA12486-9
Carnitine uptake deficiency/carnitine transport defectCopyright http://snomed.info/sct ID:21764004 Renal carnitine transport defect (disorder)	CUD	LA12487-7
Carnitine uptake deficiency/carnitine transport defect (maternal)Copyright http://snomed.info/sct ID:206001006 Fetal or neonatal effect of maternal problem unrelated to pregnancy (disorder)	CUD (mat)	LA12488-5
2,4-Dienoyl-CoA reductase deficiencyCopyright http://snomed.info/sct ID:444944006 Deficiency of 2,4-dienoyl-coenzyme A reductase (disorder)	De-Red	LA12489-3
Dihydrolipoamide dehydrogenase deficiencyCopyright http://snomed.info/sct ID:29914000 Dihydrolipoamide dehydrogenase deficiency (disorder)	E3	LA12490-1
Ethylmalonic encephalopathyCopyright http://snomed.info/sct ID:723307008 Ethylmalonic encephalopathy (disorder)	EMA	LA12491-9
Formiminoglutamic acidemiaCopyright http://snomed.info/sct ID:59761008 Glutamate formiminotransferase deficiency (disorder)	FIGLU	LA12492-7
Glutaric acidemia type ICopyright http://snomed.info/sct ID:76175005 Glutaric aciduria, type 1 (disorder)	GA-1	LA12493-5
Glutaric acidemia (maternal)Copyright http://snomed.info/sct ID:206001006 Fetal or neonatal effect of maternal problem unrelated to pregnancy (disorder)	GA-1 (mat)	LA12494-3
Glutaric acidemia type IICopyright http://snomed.info/sct ID:22886006 Glutaric aciduria, type 2 (disorder)	GA-2	LA12495-0
HomocystinuriaCopyright http://snomed.info/sct ID:11282001 Homocystinuria (disorder)	HCY	LA12496-8
Hyperornithinemia-hyperammonemia-homocitrullinuria syndromeCopyright http://snomed.info/sct ID:30287008 Hyperornithinemia-hyperammonemia-homocitrullinuria syndrome (disorder)	HHH	LA12497-6
HistidinemiaCopyright http://snomed.info/sct ID:410058007 Histidinemia (disorder)	HIS	LA12498-4
3-Hydroxy-3-methylglutaric aciduriaCopyright http://snomed.info/sct ID:410059004 Hydroxymethylglutaric aciduria (disorder)	HMG	LA12499-2
Hyperphenylalaninemia (variant, benign)Copyright http://snomed.info/sct ID:68528007 Hyperphenylalaninemia (disorder)	H-PHE	LA12500-7
HyperlysinemiaCopyright http://snomed.info/sct ID:58558003 Hyperlysinemia (disorder)	Hyper LYS	LA12501-5
Girate atrophy of the retinaCopyright http://snomed.info/sct ID:314467007 Gyrate atrophy (disorder)	Hyper ORN	LA12502-3
ValinemiaCopyright http://snomed.info/sct ID:47719001 Hypervalinemia (disorder)	Hyper VAL	LA12503-1
IsobutyrylglycinuriaCopyright http://snomed.info/sct ID:445571008 Isobutyrylglycinuria (disorder)	IBG	LA12504-9
Isovaleric acidemiaCopyright http://snomed.info/sct ID:87827003 Isovaleryl-coenzyme A dehydrogenase deficiency (disorder)	IVA	LA12505-6
Primary lactic acidemiaCopyright http://snomed.info/sct ID:190882007 Lactic acidemia (disorder)	LACTIC	LA12506-4
Long-chain L-3 hydroxyacyl-CoA dehydrogenase deficiencyCopyright http://snomed.info/sct ID:307127004 Isolated long chain hydroxyacyl-CoA dehydrogenase deficiency (disorder)	LCHAD	LA12507-2
Malonic acidemiaCopyright http://snomed.info/sct ID:124594007 Deficiency of malonyl-coenzyme A decarboxylase (disorder)	MAL	LA12508-0
Medium-chain acyl-CoA dehydrogenase deficiencyCopyright http://snomed.info/sct ID:128596003 Medium-chain acyl-coenzyme A dehydrogenase deficiency (disorder)	MCAD	LA12509-8
Holoocarboxylase synthase deficiencyCopyright http://snomed.info/sct ID:360369003 Holocarboxylase synthase deficiency (disorder)	MCD	LA12510-6
Medium-chain ketoacyl-CoA thiolase deficiencyCopyright http://snomed.info/sct ID:124265004 Deficiency of acetyl-coenzyme A acyltransferase (disorder)	MCKAT	LA12511-4
HypermethioninemiaCopyright http://snomed.info/sct ID:43123004 Hypermethioninemia (disorder)	MET	LA12512-2
Maple syrup urine diseaseCopyright http://snomed.info/sct ID:27718001 Maple syrup urine disease (disorder)	MSUD	LA21168-2
Methylene tetrahydrofolate reductase deficiencyCopyright http://snomed.info/sct ID:41797007 5,10-Methylenetetrahydrofolate reductase deficiency (disorder)	MTHFR	LA12514-8
Methylmalonic acidemiaCopyright http://snomed.info/sct ID:124680001 Deficiency of methylmalonyl-coenzyme A mutase (disorder)	MUT	LA12515-5
Nonketotic hyperglycinemia (glycine encephalopathy)Copyright http://snomed.info/sct ID:237939006 Non-ketotic hyperglycinemia (disorder)	NKHG	LA12516-3
HydroxyprolinemiaCopyright http://snomed.info/sct ID:25739007 Hyperhydroxyprolinemia (disorder)	OH PRO	LA12517-1
Ornithine transcarbamylase deficiencyCopyright http://snomed.info/sct ID:80908008 Ornithine carbamoyltransferase deficiency (disorder)	OTC	LA12518-9
Pyruvate carboxylase deficiencyCopyright http://snomed.info/sct ID:87694001 Pyruvate carboxylase deficiency (disorder)	PC	LA12519-7
Classic phenylketonuriaCopyright http://snomed.info/sct ID:7573000 Classical phenylketonuria (disorder)	PKU	LA12520-5
Hyperprolinemia type ICopyright http://snomed.info/sct ID:61071003 Proline dehydrogenase deficiency (disorder)	PRO I	LA12521-3
Hyperprolinemia type IICopyright http://snomed.info/sct ID:717181004 Hyperprolinemia type 2 (disorder)	PRO II	LA12522-1
Propionic acidemiaCopyright http://snomed.info/sct ID:69080001 Propionic acidemia (disorder)	PROP	LA12523-9
Short-chain acyl-CoA dehydrogenase deficiencyCopyright http://snomed.info/sct ID:124166007 Deficiency of butyryl-CoA dehydrogenase (disorder)	SCAD	LA12524-7
Short-chain L-3-hydroxy acyl-CoA dehydrogenase deficiencyCopyright http://snomed.info/sct ID:237998000 Short chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency (disorder)	SCHAD	LA12525-4
Succinyl-CoA ligase deficiencyCopyright http://snomed.info/sct ID:445275003 Deficiency of succinate-coenzyme A ligase (disorder)	SUCLA2	LA12526-2
Trifunctional protein deficiencyCopyright http://snomed.info/sct ID:237999008 Mitochondrial trifunctional protein deficiency (disorder)	TFP	LA12527-0
Tyrosinemia, type ICopyright http://snomed.info/sct ID:410056006 Tyrosinemia type I (disorder)	TYR-I	LA12528-8
Tyrosinemia, type IICopyright http://snomed.info/sct ID:4887000 Hypertyrosinemia, Richner-Hanhart type (disorder)	TYR-II	LA12529-6
Tyrosinemia, type IIICopyright http://snomed.info/sct ID:415764005 Tyrosinemia type III (disorder)	TYR-III	LA12530-4
Very long-chain acyl-CoA dehydrogenase deficiencyCopyright http://snomed.info/sct ID:237997005 Very long chain acyl-coenzyme A dehydrogenase deficiency (disorder)	VLCAD	LA12531-2
Biotinidase deficiencyCopyright http://snomed.info/sct ID:8808004 Biotinidase deficiency (disorder)	BIO	LA12532-0
Congenital adrenal hyperplasiaCopyright http://snomed.info/sct ID:237751000 Congenital adrenal hyperplasia (disorder)	CAH	LA12533-8
Cystic fibrosisCopyright http://snomed.info/sct ID:190905008 Cystic fibrosis (disorder)	CF	LA22202-8
Primary congenital hypothyroidismCopyright http://snomed.info/sct ID:190268003 Congenital hypothyroidism (disorder)	CH	LA12538-7
Secondary congenital hypothyroidismCopyright http://snomed.info/sct ID:82598004 Secondary hypothyroidism (disorder)	CH2	LA12539-5
Glucose-6-phosphate dehydrogenase deficiencyCopyright http://snomed.info/sct ID:124134002 Deficiency of glucose-6-phosphate dehydrogenase (disorder)	G6PD	LA12540-3
Galactoepimerase deficiencyCopyright http://snomed.info/sct ID:8849004 Uridine diphosphate glucose-4-epimerase deficiency (disorder)	GALE	LA12541-1
Galactokinase deficiencyCopyright http://snomed.info/sct ID:124302001 Deficiency of galactokinase (disorder)	GALT	LA12542-9
Classical galactosemia		LA21165-8
Hb C-carrierCopyright http://snomed.info/sct ID:76050008 Hemoglobin C trait (disorder)		LA12602-1
Hb D-carrierCopyright http://snomed.info/sct ID:7391009 Hemoglobin D trait (disorder)		LA12603-9
Hb E-carrierCopyright http://snomed.info/sct ID:46248003 Hemoglobin E trait (disorder)		LA12604-7
Hb O-Arab carrier		LA12605-4
Hb S (sickle)-carrierCopyright http://snomed.info/sct ID:16402000 Sickle cell trait (disorder)		LA12606-2
Hb C-diseaseCopyright http://snomed.info/sct ID:51053007 Hemoglobin C disease (disorder)		LA12607-0
Hb C beta-thalassemiaCopyright http://snomed.info/sct ID:119691000119106 Hemoglobin C/beta thalassemia disease (disorder)		LA12608-8
Hb D-disease		LA12609-6
Hb D beta-thalassemiaCopyright http://snomed.info/sct ID:119701000119106 Hemoglobin D/beta thalassemia disease (disorder)		LA12610-4
Hb beta zero-thalassemiaCopyright http://snomed.info/sct ID:86715000 Beta zero thalassemia (disorder)		LA12611-2
Hb E-diseaseCopyright http://snomed.info/sct ID:25065001 Hemoglobin E disease (disorder)		LA12612-0
Hb E beta-thalassemiaCopyright http://snomed.info/sct ID:234392002 Hemoglobin E/beta thalassemia disease (disorder)		LA12613-8
Hb SS-disease (sickle cell anemia)Copyright http://snomed.info/sct ID:127040003 Sickle cell-hemoglobin SS disease (disorder)		LA12614-6
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 diseaseCopyright http://snomed.info/sct ID:127048005 Sickle cell-Hemoglobin O Arab disease (disorder)		LA12619-5
Hb S plus Hb other than A,C,D,E,O-Arab diseaseCopyright http://snomed.info/sct ID:23269001 Double heterozygous sickling disorder (disorder)		LA12620-3
Hb disease other than A, C, D, E, H,O-Arab, SCopyright http://snomed.info/sct ID:80141007 Hemoglobinopathy (disorder)		LA12621-1
Hb carrier other than C, D, E, S ,O-Arab		LA12622-9
Congenital HIVCopyright http://snomed.info/sct ID:52079000 Congenital human immunodeficiency virus infection (disorder)	HIV	LA12565-0
Severe combined immunodeficiencyCopyright http://snomed.info/sct ID:31323000 Severe combined immunodeficiency disease (disorder) Severe combined immunodeficiency (SCID) is an inherited disorder of the immune system resulting from a defect in both T and B lymphocytes. Beginning in the first few months of life, affected individuals are prone to recurrent and persistent infections caused by opportunistic bacteria, viruses, and fungi. These infections are often serious or life-threatening. Researchers have described several different types of severe combined immunodeficiency, which are caused by mutations in multiple genes.	SCID	LA12566-8
Thyroid-binding globulin deficiencyCopyright http://snomed.info/sct ID:237544006 Thyroid-binding globulin deficiency (disorder)	TBG	LA12567-6
Congenital toxoplasmosisCopyright http://snomed.info/sct ID:73893000 Congenital toxoplasmosis (disorder)	TOXO	LA12568-4
CIT-I or CIT-II or ASA		LA12569-2
HCY or MET or CBL C		LA12570-0
PKU or BIPT-BS or BIOPT-REG or H-PHE		LA12571-8
TYR-1 or TYR-II or TYR-III		LA12572-6
CPT-II or CACT		LA12573-4
LCHAD or TFP		LA12574-2
MCAD or SCAD or GA-2(MADD)		LA12575-9
SCAD or EMA or IBG or GA-2 (MADD)		LA12576-7
2M3HBA or BKT-2		LA12577-5
IVA or 2MBG or GA-2 or EMA		LA12578-3
PROP or CBL A or CBL B or MUT or CBL C or MCD		LA12579-1
3-MCC or 3-MCC (mat) or 3MGA or BKT or HMG or MCD or BIO		LA12915-7
CUD or CUD (mat) or CPT-Ia		LA12916-5
GA-1 or GA-2		LA12917-3
Fabry diseaseCopyright http://snomed.info/sct ID:16652001 Fabry's disease (disorder) Fabry disease is an inherited disorder that results from the buildup of a fatty substance called globotriaosylceramide in the body's cells. This buildup leads to episodes of pain, particularly in the hands and feet; small, dark red spots on the skin called angiokeratomas; decreased sweating (hypohidrosis); corneal opacity; and hearing loss. Fabry disease can also involve potentially life-threatening complications such as progressive kidney damage, heart attack, and stroke. This disorder is caused by mutations in the GLA gene; it has an X-linked pattern of inheritance.	GLA	LA14036-0
Pompe diseaseCopyright http://snomed.info/sct ID:274864009 Glycogen storage disease due to acid maltase deficiency (disorder) Pompe disease is an inherited disorder caused by the buildup of a complex sugar called glycogen in the body's cells. The accumulation of glycogen in certain organs and tissues, especially in muscles, impairs their ability to function normally. Major features of Pompe disease include muscle weakness, heart abnormalities, and breathing problems. This disorder is caused by mutations in the GAA gene; it has an autosomal recessive pattern of inheritance.	GAA	LA14037-8
Krabbe diseaseCopyright http://snomed.info/sct ID:192782005 Galactosylceramide beta-galactosidase deficiency (disorder) Krabbe disease is an inherited disorder that affects the nervous system. This condition is characterized by severe muscle weakness, slow mental and physical development, vision loss, and seizures. Mutations in the GALC gene cause Krabbe disease; it has an autosomal recessive pattern of inheritance.	GALC	LA14038-6
Gaucher diseaseCopyright http://snomed.info/sct ID:190794006 Glucosylceramide beta-glucosidase deficiency (disorder) Gaucher disease is an inherited disorder that affects many of the body's organs and tissues. Common signs and symptoms include hepatosplenomegaly, anemia, thrombocytopenia, lung disease, and bone abnormalities. The severe types of the disease also involve the central nervous system, causing neurological problems such as abnormal eye movements, seizures, and brain damage. Gaucher disease results from mutations in the GBA gene; it has an autosomal recessive pattern of inheritance.	GBA	LA14039-4
Niemann Pick disease A/BCopyright http://snomed.info/sct ID:58459009 Sphingomyelin/cholesterol lipidosis (disorder) Niemann-Pick disease is an inherited disorder in which the body in unable to process fats and cholesterol properly. People with this condition have some combination of the following features: failure to thrive, an enlarged liver and spleen, neurological problems, frequent lung infections, an increased risk of abnormal blood clots, developmental delay, seizures, and poor muscle tone. Mutations in the SMPD1 gene causes Niemann-Pick disease; it has an autosomal recessive pattern of inheritance.	ASM	LA14040-2
Hb H-diseaseCopyright http://snomed.info/sct ID:48553001 Hemoglobin H disease (disorder)		LA16007-9
HemoglobinopathiesCopyright http://snomed.info/sct ID:80141007 Hemoglobinopathy (disorder)		LA16207-5
Critical congenital heart disease Critical congenital heart disease (CCHD) is a term that refers to a group of serious heart defects that are present from birth. These abnormalities result from problems with the formation of one or more parts of the heart during the early stages of embryonic development. CCHD prevents the heart from pumping blood effectively or reduces the amount of oxygen in the blood. As a result, organs and tissues throughout the body do not receive enough oxygen, which can lead to organ damage and life-threatening complications. Individuals with CCHD usually require surgery soon after birth.	CCHD	LA20349-9
X-linked adrenoleukodystrophyCopyright http://snomed.info/sct ID:65389002 Adrenoleukodystrophy (disorder)	X-ALD	LA25796-6
Mucopolysaccharidosis type ICopyright http://snomed.info/sct ID:75610003 Mucopolysaccharidosis type I (disorder)	MPS-I	LA25797-4
Guanidinoacetate N-methyltransferase deficiencyCopyright http://snomed.info/sct ID:124239003 Deficiency of guanidinoacetate methyltransferase (disorder)	GAMT	LA30113-7
L-arginine:glycine amidinotransferase deficiencyCopyright http://snomed.info/sct ID:702440000 Cerebral creatine deficiency syndrome 3 (disorder)	AGAT	LA30114-5
X-linked creatine transporter (CRTR) deficiencyCopyright http://snomed.info/sct ID:698290008 X-linked creatine deficiency (disorder)	CRTR	LA30492-5
Spinal muscular atrophyCopyright http://snomed.info/sct ID:5262007 Spinal muscular atrophy (disorder)	SMA	LA22279-6
Deficiency of guanidinoacetate methyltransferase (disorder)		LA34469-9
Mucopolysaccharidosis type II (disorder)		LA34470-7

Basic Attributes

Class: CHEM
Type: Laboratory
First Released: Version 2.29
Last Updated: Version 2.73
Change Reason: Changed answer list from "Normative" to "Preferred" to fit the current LOINC model.
Order vs. Observation: Observation
Common Test Rank Get Info: 17163

Member of these Panels

LOINC	Long Common Name
104191-2	Guanidinoacetate methyltransferase (GAMT) deficiency newborn screening panel
54089-8	Newborn screening panel American Health Information Community (AHIC)
57794-0	Newborn screening test results panel - DBS

Language Variants Get Info

Tag	Language	Translation
es-ES	Spanish (Spain)	Estado del recién nacido con marcadores equívocos:Presencia o identidad:Punto temporal:gota de sangre (papel de filtro):Nom:
es-MX	Spanish (Mexico)	Condiciones del recién nacido con marcadores equívocos:Presencia o identidad:Punto temporal:DBS:Nominal:
fr-FR	French (France)	Conditions néonatales avec marqueurs équivoques:Identification:Ponctuel:Sang buvard:Résultat nominal:
fr-BE	French (Belgium)	Conditions néonatales avec marqueurs équivoques:Présence ou identité:Temps ponctuel:Sang sur papier filtre:Nominal:
it-IT	Italian (Italy)	Neonato, condizioni con marcatori sospetti:Prid:Pt:Sangue.su carta da filtro:Nom: Synonyms: Chimica Condizioni del neonato con marcatori sospetti Presenza o Identità Punto nel tempo (episodio) Sangue Spot sangue secco
pt-BR	Portuguese (Brazil)	Condições de recém-nascidos com marcadores equívocos:Ident:Pt:SgPapel:Nom: Synonyms: ; NB conditions with equivocal markers; Identity or presence; Point in time; Random; DBS; Filter paper; FP; Dried blood spot; Blood; WB; Whole blood; Nominal; New born; Chemistry
ru-RU	Russian (Russian Federation)	Новорождённый состояние с неопределённые маркеры:ПрИд:ТчкВрм:Кр.Сух.капл:Ном: Synonyms: Кровь Кровь сухая капля Номинальный;Именной Присутствие или Идентификация Точка во времени;Момент
tr-TR	Turkish (Turkey)	Kuşkulu belirteçli yenidoğan şartları:MevcKimlik:Zmlı:Kan.nokta:Snf:
zh-CN	Chinese (China)	带有模糊标志的新生儿健康状况: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;身份标识带有模糊（含糊、模棱两可、不明确、含糊其词、不明）标记新生儿健康状况（状况、情况、病情）时刻;随机;随意;瞬间血;血液

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LOINC Copyright

Copyright © 2024 Regenstrief Institute, Inc. All Rights Reserved. To the extent included herein, the LOINC table and LOINC codes are copyright © 1995-2024, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee. See https://loinc.org/license for the full LOINC copyright and license.