Version 2.77

Part Descriptions

LP62864-1   FISH
FISH (fluorescence in situ hybridization) is a cytogenetic technique used to detect and localize the presence or absence of specific DNA sequences on chromosomes. FISH uses fluorescent probes that bind to only those parts of the chromosome with which they show a high degree of sequence similarity. Fluorescence microscopy can be used to find out where the fluorescent probe bound to the chromosomes. FISH is often used for finding specific features in DNA for use in genetic counseling, medicine, and species identification. FISH can also be used to detect and localize specific mRNAs within tissue samples. In this context, it can help define the spatial-temporal patterns of gene expression within cells and tissues. Copyright Text is available under the Creative Commons Attribution/Share-Alike License. See http://creativecommons.org/licenses/by-sa/3.0/ for details. Source: Wikipedia, FISH

LP96858-3   Chromosome 13+18+21+X+Y aneuploidy
Aneuploidy is an abnormal number of chromosomes, and is a type of chromosome abnormality. An extra or missing chromosome is a common cause of genetic disorders (birth defects). Some cancer cells also have abnormal numbers of chromosomes. Aneuploidy occurs during cell division when the chromosomes don't separate properly between the two cells. Chromosome abnormalities occur in 1 of 160 live births, the most common being extra chromosomes 21, 18 and 13. Copyright Text is available under the Creative Commons Attribution/Share-Alike License. See http://creativecommons.org/licenses/by-sa/3.0/ for details. Source: Wikipedia, Wikipedia

Fully-Specified Name

Component
Chromosome 13+18+21+X+Y aneuploidy
Property
Find
Time
Pt
System
Amnio fld/CVS
Scale
Nom
Method
FISH

Additional Names

Short Name
Chr 13+18+21+X+Y aneup Amn/CVS FISH
Display Name
Chr 13+18+21+X+Y aneuploidy FISH Nom (Amnio fld/CVS)
Consumer Name Alpha Get Info
Chromosome 13+18+21+X+Y aneuploidy, Amnio Fld/CVS

Basic Attributes

Class
MOLPATH
Type
Laboratory
First Released
Version 2.29
Last Updated
Version 2.73
Change Reason
Release 2.68: SYSTEM: Updated since testing can also be performed on CVS specimens.
Order vs. Observation
Both
Common Test Rank Get Info
12130

Language Variants Get Info

Tag Language Translation
es-ES Spanish (Spain) Aneuploidía cromosoma 13+18+21+X+Y:Hallazgo:Punto temporal:Líquido amniótico o muestra de vellosidades coriónicas:Nom:Hibridación in situ fluoresente (FISH)
es-MX Spanish (Mexico) Cromosoma 13 + 18 + 21 + X + Y aneuploidía:Hallazgo:Punto temporal:Muestra de líquido amniótico o vellosidades coriónicas:Nominal:Hibridación fluorescente in situ (FISH)
fr-FR French (France) Chromosome 13+18+21+X+Y aneuploïdie:Recherche:Ponctuel:Liquide amniotique/Villosités choriales:Résultat nominal:FISH
it-IT Italian (Italy) Cromosoma 13+18+21+X+Y, aneuploidia:Osservazione:Pt:Liquido amniotico/Villi coriali, prelievo:Nom:FISH
Synonyms: Aneuploidia del cromosoma 13+18+21+X+Y Campione di villi coriali Ibridazione in situ fluorescente (FISH) Liquido amniotico Osservazione Patologia molecolare Prelievo del liquido amniotico o dei villi coriali Punto nel tempo (episodio)
pt-BR Portuguese (Brazil) Chromosome 13+18+21+X+Y aneuploidia:Achado:Pt:LiqAmni:Nom:FISH (hibridização in situ fluorescente)
Synonyms: ; Chrom 13+18+21+X+Y aneuploidy; Chromosomes; Finding; Findings; Point in time; Random; Amn; Amniotic fluid; Amn fl; Amniotic flu; AF; Nominal; Fluorescent in situ hybridization; Chromosom; Molecular pathology
tr-TR Turkish (Turkey) Kromozom 13+18+21+X+Y anöploidy:Bulgu:Zmlı:Amnio sv/CVS:Snf:FISH
Synonyms: Amniyon mayii
uk-UA Ukrainian (Ukraine) Хромосома 13+18+21+X+Y анеуплоїдія:Знахідка:МоментЧасу:Амніотична рідина/Проба ворсин хоріона:Категорійно:Флуоресцентна гібридизація in situ (FISH)
Synonyms: AF; Amn; Amn fl; Amn/CVS; Amnio; Amniotic flu; Amniotic fluid; Chorionic villi; Chorionic villus sample; Chr 13+18+21+X+Y aneup; Chromosom; Chromosomes; Finding; Findings; Fluorescent in situ hybridization; Genetics; Gyn; Gynecology; Heredity; Heritable; Inherited; Molecular pathology; MOLPATH; Nominal; OB; ObGyn; Obstetrics; Point in time; Random
zh-CN Chinese (China) 染色体 13+18+21+X+Y 非整倍体性:发现:时间点:羊水/绒毛膜绒毛样本:名义型:FISH
Synonyms: 13+18+21+X+Y 染色体非整倍体型;13+18+21+X+Y 染色体非整倍性;染色体 13+18+21+X+Y 非整倍体性(非整倍体型、非整倍体、异倍体、非整倍性、异倍性、非整倍态、异倍体性) Fluorescent in situ hybridization;荧光原位杂交 分子病理学;分子病理学试验 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 发现是一个原子型临床观察指标,并不是作为印象的概括陈述。体格检查、病史、系统检查及其他此类观察指标的属性均为发现。它们的标尺对于编码型发现可能是名义型,而对于叙述型文本之中所报告的发现,则可能是叙述型。;发现物;所见;结果;结论 时刻;随机;随意;瞬间 染色体二体型+染色体三体型 绒毛膜绒毛标本;绒膜绒毛标本;绒膜绒毛样本 羊水(羊膜水、胎水)或绒毛膜绒毛样本(绒毛膜绒毛标本、绒膜绒毛标本、绒膜绒毛样本、CVS) 羊膜水;胎水

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CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=57317-0