75384-8LOINC 2.82
PMP22 gene deletion and duplication mutation analysis in Blood or Tissue by MLPA
PMP22 gene Del+Dup Bld/T MLPA
Component
- PMP22 gene deletion+duplication
Specimen / system
- Bld/Tiss
Class
- MOLPATH.DEL
Property
- Find
Scale
- Doc
Method
- MLPA
Related names
- Amplification; Blood; Charcot-Marie Tooth disease; CMT; CMT1A; CMT1E; Dejerine-Sottas syndrome; Del; Del+Dup; Deletions; Document; Dp; DSS; Finding; Findings; GAS3; GAS-3; Growth arrest specific gene 3; Hereditary neuropathy with liability to pressure palsies; HMSNIA; HNPP; Molecular pathology; MOLPATH; MOLPATH.DELETIONS; peripheral myelin protein 22; PMP-22; Point in time; Random; Sp110; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Amplification
- Blood
- Charcot-Marie Tooth disease
- CMT
- CMT1A
- CMT1E
- Dejerine-Sottas syndrome
- Del
- Del+Dup
- Deletions
- Document
- Dp
- DSS
- Finding
- Findings
- GAS-3
- GAS3
- Growth arrest specific gene 3
- Hereditary neuropathy with liability to pressure palsies
- HMSNIA
- HNPP
- Molecular pathology
- MOLPATH
- MOLPATH.DELETIONS
- peripheral myelin protein 22
- PMP-22
- PMP22 gene deletion+duplication
- Point in time
- Random
- Sp110
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue