57030-9

Chromosome 13+18+21+X+Y aneuploidy in Blood by Molecular genetics method Nominal

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Part Description

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

LOINC Names Get Info

Fully-Specified Name: Chromosome 13+18+21+X+Y aneuploidy:Find:Pt:Bld:Nom:Molgen
Long Common Name: Chromosome 13+18+21+X+Y aneuploidy in Blood by Molecular genetics method Nominal
Short Name: Chr 13+18+21+X+Y aneup Bld
Display Name: Chr 13+18+21+X+Y aneuploidy Molgen Nom (Bld)
Consumer Name Alpha Get Info: Chromosome 13+18+21+X+Y aneuploidy, Blood

Part Model Get Info

Component
Chromosome 13+18+21+X+Y aneuploidy
LP96858-3
- Analyte
  Chromosome 13+18+21+X+Y aneuploidy
  LP96858-3
  - Component Numerator
    Chromosome 13+18+21+X+Y aneuploidy
    LP96858-3
    - Component Numerator Core
      Chromosome 13+18+21+X+Y aneuploidy
      LP96858-3
    - Component Numerator Core Suffix
      NULL
  - Component Denominator
    NULL
    - Component Denominator Core
      NULL
    - Component Denominator Core Suffix
      NULL
- Challenge
  NULL
- Adjustment
  NULL
- Count
  NULL
Property
Find
LP6813-2
Time
Pt
LP6960-1
- Time Core
  Pt
  LP6960-1
- Time Modifier
  NULL
System
Bld
LP7057-5
- System Core
  Bld
  LP7057-5
- Super System
  NULL
Scale
Nom
LP7750-5
Method
Molgen
LP6404-0

Basic Attributes

Class: MOLPATH
Type: Laboratory
First Released: Version 2.29
Last Updated: Version 2.66 (MIN)
Order vs. Observation: Both

Language Variants Get Info

Tag	Language	Translation
cs-CZ	Czech (Czechia)	Chromozom 13+18+21+X+Y aneuploidie:Nález:Časový bod:Krev:Nominální:Molekulární genetika
el-GR	Greek (Greece)	Ανευπλοειδία χρωμοσωμάτων 13+18+21+X+Y:Εύρεση:Pt:Αίμα:Nom:Μοριακή γενετική Synonyms: MOLPATH Nom Pt Αίμα Ανευπλοειδία χρωμοσωμάτων 13+18+21+X+Y Εύρεση Μοριακή γενετική Χρωμόσωμα
es-ES	Spanish (Spain)	Aneuploidía cromosoma 13+18+21+X+Y:Hallazgo:Punto temporal:Sangre:Nom:Genética molecular
es-MX	Spanish (Mexico)	Cromosoma 13 + 18 + 21 + X + Y aneuploidía:Hallazgo:Punto temporal:Sangre:Nominal:Genética molecular
fr-CA	French (Canada)	Chromosome 13+ 18+ 21+ X+ Y aneuploïdie:Observation:Temps ponctuel:Sang:Nominal:Molgen
fr-FR	French (France)	Chromosome 13+18+21+X+Y aneuploïdie:Recherche:Ponctuel:Sang:Résultat nominal:Biologie moléculaire
it-IT	Italian (Italy)	Cromosoma 13+18+21+X+Y, aneuploidia:Osservazione:Pt:Sangue:Nom:Molgen Synonyms: Aneuploidia del cromosoma 13+18+21+X+Y Genetica molecolare Osservazione Patologia molecolare Punto nel tempo (episodio) Sangue
nl-NL	Dutch (Netherlands)	chromosoom 13+18+21+X+Y aneuploïdie:bevinding:moment:bloed:nominaal:moleculair genetisch onderzoek Synonyms: molgen
pl-PL	Polish (Poland)	Aneuploidia chromosomów 13+18+21+X+Y:stwierdzenie:punkt w czasie:krew:skala nominalna:genetyka molekularna Synonyms: diagnostyka molekularna wynik kategorialny
pt-BR	Portuguese (Brazil)	Cromossomo 13+18+21+X+Y aneuploidia:Achado:Pt:SgTotal:Nom:Genética molecular Synonyms: ; Chrom 13+18+21+X+Y aneuploidy; Chromosomes; Finding; Findings; Point in time; Random; Blood; WB; Whole blood; Nominal; PCR; Molecular genetics; Chromosom; Molecular pathology
ru-RU	Russian (Russian Federation)	Хромосома 13+18+21+X+Y анеуплоидия:Находка:ТчкВрм:Кр:Ном:МолГен Synonyms: Кровь Номинальный;Именной Точка во времени;Момент
tr-TR	Turkish (Turkey)	Kromozom 13+18+21+X+Y anöploidy:Bulgu:Zmlı:Kan:Snf:Molgen
zh-CN	Chinese (China)	染色体 13+18+21+X+Y 非整倍体性:发现:时间点:全血:名义型:分子遗传学类实验室方法 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）分子病理学;分子病理学试验分子遗传学;分子遗传学方法;分子遗传学类方法;分子遗传学类检验方法;包括 RFL、PCR 及其他方法在内，用于在分子基础上检测遗传属性的方法的大类;聚合酶链反应;聚合酶链式反应分类型应答;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+染色体三体型血;血液

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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://loinc.org/license for the full LOINC copyright and license.