34514-0LOINC 2.82
SLC22A18 gene targeted mutation analysis in Blood or Tissue by Molecular genetics method
SLC22A18 gene Mut Anl Bld/T
Component
- SLC22A18 gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Find
Scale
- Doc
Method
- Molgen
Related names
- Beckwith-Wiedemann syndrome chromosome region 1, candidate a; Blood; BWR1A; BWSCR1A; Document; Finding; Findings; Genetics; Heredity; Heritable; HET; imprinted polyspecific membrane transporter 1; IMPT1; Inherited; ITM; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; ORCTL2; organic cation transporter-like 2; p45-BWR1A; PCR; Point in time; Random; SLC22A1L; Solute carrier family 22 (organic cation transporter), member 18; solute carrier family 22 (organic cation transporter), member 1-like; solute carrier family 22, member 18; Tissue; Tissue, unspecified; TSSC5; WB; Whole blood; Whole blood or Tissue
Index terms
- Beckwith-Wiedemann syndrome chromosome region 1, candidate a
- Blood
- BWR1A
- BWSCR1A
- Document
- Finding
- Findings
- Genetics
- Heredity
- Heritable
- HET
- imprinted polyspecific membrane transporter 1
- IMPT1
- Inherited
- ITM
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- ORCTL2
- organic cation transporter-like 2
- p45-BWR1A
- PCR
- Point in time
- Random
- SLC22A1L
- solute carrier family 22 (organic cation transporter), member 1-like
- Solute carrier family 22 (organic cation transporter), member 18
- solute carrier family 22, member 18
- Tissue
- Tissue, unspecified
- TSSC5
- WB
- Whole blood
- Whole blood or Tissue