41064-7LOINC 2.82
PYGM gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
PYGM gene Mut Anl Bld/T
Component
- PYGM gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; Genetics; Glycogen phosphorylase, muscle form; Glycogen storage disease type V; Heredity; Heritable; Identity or presence; Inherited; McArdle syndrome; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Myophosphorylase gene; Nominal; PCR; phosphorylase, glycogen, muscle; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- Genetics
- Glycogen phosphorylase, muscle form
- Glycogen storage disease type V
- Heredity
- Heritable
- Identity or presence
- Inherited
- McArdle syndrome
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Myophosphorylase gene
- Nominal
- PCR
- phosphorylase, glycogen, muscle
- Point in time
- PYGM gene targeted mutation analysis
- Random
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue