41080-3LOINC 2.82
Myotonic dystrophy gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
MMD gene Mut Anl Bld/T
Component
- Myotonic dystrophy gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; DM; Genetics; Heredity; Heritable; Identity or presence; Inherited; MMD; MMD gene; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Myotonic muscular dystrophy; Nominal; PCR; Point in time; PROMM; Proximal myotonic myopathy; Random; Steinert disease; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- DM
- Genetics
- Heredity
- Heritable
- Identity or presence
- Inherited
- MMD
- MMD gene
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Myotonic dystrophy gene targeted mutation analysis
- Myotonic muscular dystrophy
- Nominal
- PCR
- Point in time
- PROMM
- Proximal myotonic myopathy
- Random
- Steinert disease
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue