41056-3

LOINC 2.82

SLC22A18 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

SLC22A18 gene Mut Anl Bld/T

Component

  • SLC22A18 gene targeted mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • Beckwith-Wiedemann syndrome chromosome region 1, candidate a; Blood; BWR1A; BWSCR1A; Genetics; Heredity; Heritable; HET; Identity or presence; imprinted polyspecific membrane transporter 1; IMPT1; Inherited; ITM; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; 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
  • Genetics
  • Heredity
  • Heritable
  • HET
  • Identity or presence
  • imprinted polyspecific membrane transporter 1
  • IMPT1
  • Inherited
  • ITM
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mut Anl
  • Mutations
  • Nominal
  • ORCTL2
  • organic cation transporter-like 2
  • p45-BWR1A
  • PCR
  • Point in time
  • Random
  • SLC22A18 gene targeted mutation analysis
  • 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