38920-5LOINC 2.82
MFN2 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
MFN2 gene Mut Anl Bld/T
Component
- MFN2 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; Charcot-Marie Tooth disease, type 2A; CMT2A; CMT2A2; CPRP1; Genetics; Heredity; Heritable; HSG; Identity or presence; Inherited; KIAA0214; MARF; Mitochondrial assembly regulatory factor; Mitofusin 2; 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
- Blood
- Charcot-Marie Tooth disease, type 2A
- CMT2A
- CMT2A2
- CPRP1
- Genetics
- Heredity
- Heritable
- HSG
- Identity or presence
- Inherited
- KIAA0214
- MARF
- MFN2 gene targeted mutation analysis
- Mitochondrial assembly regulatory factor
- Mitofusin 2
- 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