35294-8
PYGM gene targeted mutation analysis in Blood or Tissue by Molecular genetics method
Active
Part Description
LP33143-6 PYGM gene
The PYGM gene (phosphorylase, glycogen, muscle) [HGNC Gene ID:9726] is located on chromosome 11q12-q13.2. This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Sep 2009] [NCBI Gene ID:5837]
Source: National Center for Biotechnology Information (NCBI) Gene
LOINC Names Get Info
- Fully-Specified Name
- PYGM gene targeted mutation analysis:
Find: Pt: Bld/Tiss: Doc: Molgen - Long Common Name
- PYGM gene targeted mutation analysis in Blood or Tissue by Molecular genetics method
- Short Name
- PYGM gene Mut Anl Bld/T
- Display Name
- PYGM gene targeted mutation analysis Molgen Doc (Bld/Tiss)
- Consumer Name Alpha Get Info
- PYGM gene targeted mutation analysis, Blood or tissue specimen
Part Model Get Info
- Component
- PYGM gene targeted mutation analysis
LP229448-8
- Analyte
- PYGM gene targeted mutation analysis
LP229448-8
- Component Numerator
- PYGM gene targeted mutation analysis
LP229448-8
- 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/Tiss
LP7061-7
- System Core
- Bld/Tiss
LP7061-7
- Super System
- NULL
- Scale
- Doc
LP32888-7
- Method
- Molgen
LP6404-0
Basic Attributes
- Class
- MOLPATH.MUT
- Type
- Laboratory
- First Released
- Version 2.13
- Last Updated
- Version 2.73 (MIN)
- 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.; Based on LOINC Committee review (June 2019), updated the Property from "Prid" to "Find" and Scale from "Nar" to "Doc" to align with the current LOINC model for naming collections of information reported in narrative and/or structured formats.
- Order vs. Observation
- Both
- Common Test Rank Get Info
- 16604
Language Variants Get Info
| Tag | Language | Translation |
|---|---|---|
| cs-CZ | Czech (Czechia) | Gen PYGM cílená mutační analýza: |
| el-GR | Greek (Greece) | Γονίδιο PYGM στοχευμένη ανάλυση μεταλλάξεων: Synonyms: Doc MOLPATH MOLPATH.MUT Pt Αίμα Αίμα/Ιστός Γονίδιο Γονίδιο PYGM Εύρεση Ιστός Μοριακή γενετική στοχευμένη ανάλυση μεταλλάξεων |
| es-AR | Spanish (Argentina) | gen PYGM: |
| es-ES | Spanish (Spain) | Gen PYGM Analisis de mutaciones: |
| es-MX | Spanish (Mexico) | Análisis de mutaciones dirigidas al gen PYGM: |
| fr-FR | French (France) | PYGM gène mutation cible trouvée: |
| it-IT | Italian (Italy) | PYGM, gene analisi di mutazione mirata: Synonyms: Gene PYGM Genetica molecolare Mutazione genica Osservazione Patologia molecolare Punto nel tempo (episodio) Sangue Sangue o Tessuto Tessuto & |
| ko-KR | Korean (Korea, Republic Of) | PYGM 유전자 돌연변이 분석: |
| nl-NL | Dutch (Netherlands) | PYGM-gen doelgerichte mutatie-analyse: Synonyms: molgen PYGM gen targeted |
| pl-PL | Polish (Poland) | PYGM gen ukierunkowana analiza mutacji: Synonyms: Analiza mutacji genu PYGM diagnostyka molekularna Gen PYGM |
| pt-BR | Portuguese (Brazil) | PYGM análise de mutação genética: Synonyms: Myophosphorylase gene; |
| ru-RU | Russian (Russian Federation) | PYGM ген исследование на мутацию: Synonyms: Документ Кровь Кровь или Ткань Ткань и мазки Точка во времени; |
| tr-TR | Turkish (Turkey) | PYGM geni Mutasyon analizi: |
| zh-CN | Chinese (China) | PYGM 基因 突变分析: Synonyms: Glycogen-heart syndrome; |
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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://