41108-2

LOINC 2.82

FGF23 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

FGF23 gene Mut Anl Bld/T

Component

  • FGF23 gene targeted mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • ADHR; Blood; FGF-23; FGFN; Fibroblast growth factor 23; Genetics; Heredity; Heritable; HPDR2; HYPF; Hypophosphatemia vitamin D-resistant rickets-2 (autosomal dominant); Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; PCR; PHPTC; Point in time; Random; Tissue; Tissue, unspecified; Tumor-derived hypophosphatemia inducing factor; WB; Whole blood; Whole blood or Tissue

Index terms

  • ADHR
  • Blood
  • FGF-23
  • FGF23 gene targeted mutation analysis
  • FGFN
  • Fibroblast growth factor 23
  • Genetics
  • Heredity
  • Heritable
  • HPDR2
  • HYPF
  • Hypophosphatemia vitamin D-resistant rickets-2 (autosomal dominant)
  • Identity or presence
  • Inherited
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mut Anl
  • Mutations
  • Nominal
  • PCR
  • PHPTC
  • Point in time
  • Random
  • Tissue
  • Tissue, unspecified
  • Tumor-derived hypophosphatemia inducing factor
  • WB
  • Whole blood
  • Whole blood or Tissue