Version 2.77

Term Description

Multigene analysis for both syndromic and non-syndromic forms of hearing loss. Genetic forms of hearing loss may be classified as autosomal dominant, recessive, X-linked or mitochondrial. Determining the cause of hearing loss, whether it is acquired or genetic, is useful for diagnosis, prognosis, and determining treatment options for the patient.[NCBI Books: NBK1434]
Source: Regenstrief LOINC

Fully-Specified Name

Component
Hearing loss multigene analysis
Property
Find
Time
Pt
System
Bld/Tiss
Scale
Doc
Method
Molgen

Additional Names

Short Name
Hearing loss multigene analy Bld/T
Display Name
Hearing loss multigene analysis Molgen Doc (Bld/Tiss)
Consumer Name Alpha Get Info
Hearing loss multigene analysis, Blood or tissue specimen

Basic Attributes

Class
MOLPATH
Type
Laboratory
First Released
Version 2.72
Last Updated
Version 2.72
Order vs. Observation
Both

Language Variants Get Info

Tag Language Translation
es-ES Spanish (Spain) Análisis multigénico de pérdida auditiva:Hallazgo:Punto temporal:Sangre o tejido:Doc:Genética molecular
fr-FR French (France) Analyse multigénique d'une perte auditive:Recherche:Ponctuel:Sang/Tissu:Document:Biologie moléculaire
it-IT Italian (Italy) Perdita di udito, analisi multigene:Osservazione:Pt:Sangue/Tess:Doc:Molgen
Synonyms: Analisi multigene perdita di udito Genetica molecolare Osservazione Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & Strisci
nl-NL Dutch (Netherlands) multigen-analyse op gehoorverlies:bevinding:moment:bloed of weefsel:document:moleculair genetisch onderzoek
Synonyms: molgen
zh-CN Chinese (China) 听力减退多基因分析:发现:时间点:全血/组织:文档型:分子遗传学类实验室方法
Synonyms: 临床文档型;临床文档;文档;文书;医疗文书;临床医疗文书 全血或组织;血液/组织;血液或组织 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 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 听力减退（听力损失、听力丧失、失聪）多基因分析 听力损害;听力丧失;听觉损耗 听觉 时刻;随机;随意;瞬间 未作说明的组织;组织;组织 & 涂片 血;血液

LOINC Terminology Service (API) using HL7® FHIR® Get Info

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=99972-2