39089-8LOINC 2.82
PLP1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
PLP1 gene Mut Anl Bld/T
Component
- PLP1 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- Blood; Genetics; GPM6C; Heredity; Heritable; HLD1; Identity or presence; Inherited; Lipophilin; Major myelin proteolipid protein gene; MMPL; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; PCR; Pelizaeus-Merzbacher disease, spastic paraplegia 2, uncomplicated; PLP; PLP/DM20; PMD; Point in time; proteolipid protein 1; Random; SPG2; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- Genetics
- GPM6C
- Heredity
- Heritable
- HLD1
- Identity or presence
- Inherited
- Lipophilin
- Major myelin proteolipid protein gene
- MMPL
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Nominal
- PCR
- Pelizaeus-Merzbacher disease, spastic paraplegia 2, uncomplicated
- PLP
- PLP/DM20
- PLP1 gene targeted mutation analysis
- PMD
- Point in time
- proteolipid protein 1
- Random
- SPG2
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue