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Part Descriptions

LP31878-9   NPHS1 gene
The NPHS1 gene (nephrosis 1, congenital, Finnish type (nephrin)) [HGNC Gene ID:7908] is located on chromosome 19q13.1. This gene encodes a member of the immunoglobulin family of cell adhesion molecules that functions in the glomerular filtration barrier in the kidney. The gene is primarily expressed in renal tissues, and the protein is a type-1 transmembrane protein found at the slit diaphragm of glomerular podocytes. The slit diaphragm is thought to function as an ultrafilter to exclude albumin and other plasma macromolecules in the formation of urine. Mutations in this gene result in Finnish-type congenital nephrosis 1, characterized by severe proteinuria and loss of the slit diaphragm and foot processes.[provided by RefSeq, Oct 2009] [NCBI Gene ID:4868] Source: National Center for Biotechnology Information (NCBI) Gene

LP7238-1   Body fld
The LOINC "Body fld" System represents body fluids other than serum, plasma, blood, urine, and cerebrospinal fluid. When a LOINC term with the System "Body fld" is used, the specific specimen source or body fluid type should be reported elsewhere with the result. Where more specific terms for pleural, peritoneal, synovial fluid, etc. exist, we encourage you to use the more specific terms. In contrast to "Body fld", the System "Asp" in LOINC represents the fluid withdrawn during an aspiration procedure from an abnormal collection of fluid, such as from an abscess or cyst. "Asp" is used for abnormal fluid collections that are aspirated, while "Body fld" is used for named body fluids, such as synovial fluid or peritoneal fluid, that are not inherently pathologic. Source: Regenstrief LOINC

LOINC Names Get Info

Fully-Specified Name
NPHS1 gene mutations:Prid:Pt:Body fld:Nom:Targeted gene mutation analysis
Long Common Name
NPHS1 gene mutations found [Identifier] in Body fluid by Targeted gene mutation analysis Nominal
Short Name
NPHS1 gene Mut Fld Mut Anl
Display Name
NPHS1 gene mutations found Targeted gene mutation analysis Nom (Body fld)
Consumer Name Alpha Get Info
NPHS1 gene mutations found, Body fluid

Part Model Get Info

  • Component
    NPHS1 gene mutations
    LP452030-2
    • Analyte
      NPHS1 gene mutations
      LP452030-2
      • Component Numerator
        NPHS1 gene mutations
        LP452030-2
      • Component Denominator
        NULL
         
        • Component Denominator Core
          NULL
           
        • Component Denominator Core Suffix
          NULL
           
    • Challenge
      NULL
       
    • Adjustment
      NULL
       
    • Count
      NULL
       
  • Property
    Prid
    LP6850-4
  • Time
    Pt
    LP6960-1
  • System
    Body fld
    LP7238-1
    • System Core
      Body fld
      LP7238-1
    • Super System
      NULL
       
  • Scale
    Nom
    LP7750-5
  • Method
    Targeted gene mutation analysis
    LP95475-7

Basic Attributes

Class
MOLPATH.MUT
Type
Laboratory
First Released
Version 2.15
Last Updated
Version 2.83 (NAM)
Change Reason
Based on LOINC Committee review (June 2016), "targeted" was added to the Component to clarify that this test is looking for a specific set of mutations as described in the LOINC User Guide under the Molecular Genetics section.
Order vs. Observation
Both

Language Variants Get Info

TagLanguageTranslation
cs-CZCzech (Czechia)Gen NPHS1 cílená mutační analýza:Přítomnost nebo identita:Časový bod:Tělní tekutina:Nominální:Molekulární genetika
el-GRGreek (Greece)Γονίδιο NPHS1 στοχευμένη ανάλυση μεταλλάξεων:Prid:Pt:Σωματικό υγρό:Nom:Μοριακή γενετική
Synonyms: MOLPATH MOLPATH.MUT Nom Prid Pt Γονίδιο Γονίδιο NPHS1 Μοριακή γενετική στοχευμένη ανάλυση μεταλλάξεων Σωματικό υγρό
es-ESSpanish (Spain)Gen NPHS1 Analisis de mutaciones:Presencia o identidad:Punto temporal:Fluido corporal:Nom:Genética molecular
es-MXSpanish (Mexico)Análisis de mutaciones dirigidas al gen NPHS1:Presencia o identidad:Punto temporal:Fluído corporal:Nominal:Genética molecular
fr-FRFrench (France)NPHS1 gène mutation cible trouvée:Identification:Ponctuel:Liquide biologique:Résultat nominal:Biologie moléculaire
it-ITItalian (Italy)NPHS1, gene analisi di mutazione mirata:Prid:Pt:Liquido corporeo:Nom:Molgen
Synonyms: Gene NPHS1 Genetica molecolare Liquido corporeo Mutazione genica Patologia molecolare Presenza o Identità Punto nel tempo (episodio)
ko-KRKorean (Korea, Republic Of)NPHS1 유전자 돌연변이 분석:존재:검사시점:체액:명칭결과:분자유전
nl-NLDutch (Netherlands)NPHS1-gen doelgerichte mutatie-analyse:identificator:moment:lichaamsvocht:nominaal:moleculair genetisch onderzoek
Synonyms: molgen NPHS1 gen targeted
pl-PLPolish (Poland)NPHS1 gen ukierunkowana analiza mutacji:obecność lub identyfikacja:punkt w czasie:płyn ustrojowy:skala nominalna:genetyka molekularna
Synonyms: Analiza mutacji genu NPHS1 diagnostyka molekularna Gen NPHS1 wynik kategorialny
pt-BRPortuguese (Brazil)NPHS1 análise de mutação genética:Ident:Pt:LiqOrg:Nom:Genética molecular
Synonyms: nephrosis 1, congenital, Finnish type; CNF; NPHN; Nephrin; Identity or presence; Point in time; Random; BF; Fluid; Body fluid; FLU; Fl; Nominal; PCR; Molecular genetics; Mut Anal; Mutations; MOLPATH.MUTATIONS; MOLPATH.MUTATIONS; Molecular pathology
ru-RURussian (Russian Federation)NPHS1 ген исследование на мутацию:ПрИд:ТчкВрм:Тело ждк:Ном:МолГен
Synonyms: Номинальный;Именной Присутствие или Идентификация Тела жидкость Точка во времени;Момент
tr-TRTurkish (Turkey)NPHS1 geni Mutasyon analizi:MevcKimlik:Zmlı:Vücut sv:Snf:Molgen
zh-CNChinese (China)NPHS1 基因 突变分析:存在与否或特征标识:时间点:体液:名义型:分子遗传学类实验室方法
Synonyms: CNF;Nephrin;Nephrin（肾小球裂孔膜上发现的第一个跨膜蛋白,是细胞粘附分子中的免疫球蛋白超家族成员,参与肾脏滤过屏障的正常发育并维持其正常功能）;NPHN;肾病 1, 先天性, Finnish 型;肾病 1, 先天性, 芬兰型;芬兰型先天性肾病综合征;裂孔跨膜蛋白;裂孔跨膜蛋白 Nephrin;裂孔隔膜蛋白;裂孔隔膜蛋白 Nephrin 分子病理学.基因突变;分子病理学.突变;分子病理学试验.基因突变;分子病理学试验.突变;分子病理学试验类.突变;基因突变;突变 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 基因突变分析 存在;存在与否;特征标识;身份;身份标识 时刻;随机;随意;瞬间 物体 遗传基因;遗传因子;吉恩;生物基因

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

CodeSystem lookup
https://fhir.loinc.org/CodeSystem/$lookup?system=http://loinc.org&code=41074-6