41112-4LOINC 2.82
CMT axonal gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
CMT2 gene Mut Anl Bld/T
Component
- CMT axonal gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Axonal HMSN; Blood; Charcot-Marie Tooth disease, type 2; CMT; CMT2; CMT2 gene; Genetics; GJB, MPZ and NEFL gene mutations; Heredity; Heritable; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Axonal HMSN
- Blood
- Charcot-Marie Tooth disease, type 2
- CMT
- CMT axonal gene targeted mutation analysis
- CMT2
- CMT2 gene
- Genetics
- GJB, MPZ and NEFL gene mutations
- Heredity
- Heritable
- Identity or presence
- Inherited
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Nominal
- PCR
- Point in time
- Random
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue