73748-6

LOINC 2.82

APOB gene p.Arg3500Gln and p.Arg3500Trp [Identifier] in Blood or Tissue by Molecular genetics method Nominal

APOB R3500Q+R3500W Bld/T

Component

  • APOB gene.p.Arg3500Gln & Arg3500Trp

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • Apo B; ApoB; APOB R3500Q+R3500W; ApoB-100; apolipoprotein B; Apolipoprotein B gene; Autosomal dominant hypercholesterolemia; Blood; Familial defective apolipoprotein B-100; FDB; FLDB; Genetics; Heredity; Heritable; Identity or presence; Inherited; LDLCQ4; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Nominal; P prime; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Index terms

  • Apo B
  • ApoB
  • APOB gene.p.Arg3500Gln & Arg3500Trp
  • APOB R3500Q+R3500W
  • ApoB-100
  • apolipoprotein B
  • Apolipoprotein B gene
  • Autosomal dominant hypercholesterolemia
  • Blood
  • Familial defective apolipoprotein B-100
  • FDB
  • FLDB
  • Genetics
  • Heredity
  • Heritable
  • Identity or presence
  • Inherited
  • LDLCQ4
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Nominal
  • P prime
  • PCR
  • Point in time
  • Random
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue