40970-6
VWF gene mutations found [Identifier] in Blood or Tissue by Targeted gene mutation analysis Nominal
Active
Part Description
LP35694-6 VWF gene
The VWF gene (von Willebrand factor) [HGNC Gene ID:12726] is located on chromosome 12p13.3. The glycoprotein encoded by this gene functions as both an antihemophilic factor carrier and a platelet-vessel wall mediator in the blood coagulation system. It is crucial to the hemostasis process. Mutations in this gene or deficiencies in this protein result in von Willebrand's disease. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq, Jul 2008] [NCBI Gene ID:7450]
Source: National Center for Biotechnology Information (NCBI) Gene
LOINC Names Get Info
- Fully-Specified Name
- VWF gene mutations:
Prid: Pt: Bld/Tiss: Nom: Targeted gene mutation analysis - Long Common Name
- VWF gene mutations found [Identifier] in Blood or Tissue by Targeted gene mutation analysis Nominal
- Short Name
- VWF gene Mut Bld/T Mut Anl
- Display Name
- VWF gene mutations found Targeted gene mutation analysis Nom (Bld/Tiss)
- Consumer Name Alpha Get Info
- VWF gene mutations found, Blood or tissue specimen
Part Model Get Info
- Component
- VWF gene mutations
LP451997-3
- Analyte
- VWF gene mutations
LP451997-3
- Component Numerator
- VWF gene mutations
LP451997-3
- Component Numerator Core
- VWF gene
LP35694-6
- Component Numerator Core Suffix
- mutations
LP452208-4
- 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
- Time Core
- Pt
LP6960-1
- Time Modifier
- NULL
- System
- Bld/Tiss
LP7061-7
- System Core
- Bld/Tiss
LP7061-7
- 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
- Common Test Rank Get Info
- 13780
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| cs-CZ | Czech (Czechia) | Gen VWF cílená mutační analýza: |
| el-GR | Greek (Greece) | Γονίδιο VWF στοχευμένη ανάλυση μεταλλάξεων: Synonyms: MOLPATH MOLPATH.MUT Nom Prid Pt Αίμα Αίμα/Ιστός Γονίδιο Γονίδιο VWF Ιστός Μοριακή γενετική στοχευμένη ανάλυση μεταλλάξεων |
| es-ES | Spanish (Spain) | Gen VWF Analisis de mutaciones: |
| es-MX | Spanish (Mexico) | Análisis de mutaciones dirigidas al gen del FvW: |
| fr-FR | French (France) | VWF gène mutation cible trouvée: |
| it-IT | Italian (Italy) | VWF, gene analisi di mutazione mirata: Synonyms: Gene VWF Genetica molecolare Mutazione genica Patologia molecolare Presenza o Identità Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & |
| ko-KR | Korean (Korea, Republic Of) | VWF 유전자 돌연변이 분석: |
| nl-NL | Dutch (Netherlands) | VWF-gen doelgerichte mutatie-analyse: Synonyms: molgen targeted VWF gen |
| pl-PL | Polish (Poland) | VWF gen ukierunkowana analiza mutacji: Synonyms: Analiza mutacji genu czynnika von Willebranda diagnostyka molekularna Gen VWF wynik kategorialny |
| pt-BR | Portuguese (Brazil) | WWF análise de mutação genética: Synonyms: von Willebrand Factor gene; |
| ru-RU | Russian (Russian Federation) | VWF ген исследование на мутацию: Synonyms: Кровь Кровь или Ткань Номинальный; |
| tr-TR | Turkish (Turkey) | VWF geni Mutasyon analizi: |
| zh-CN | Chinese (China) | VWF 基因 突变分析: Synonyms: F8VWF; |
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LOINC Copyright
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://