45190-6

LOINC 2.82

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

CASR gene Mut Anl Bld/T

Component

  • CASR gene targeted mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • Blood; calcium-sensing receptor; Calcium-sensing receptor (hypocalciuric hypercalcemia 1, severe neonatal hyperparathyroidism); CAR; CaSR; EIG8; Extracellular calcium-sensing receptor precursor; FHH; FIH; Genetics; GPRC2A; Heredity; Heritable; HHC; HHC1; HYPOC1; Identity or presence; Inherited; MGC138441; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; NSHPT; Parathyroid Cell calcium-sensing receptor; PCAR1; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Index terms

  • Blood
  • calcium-sensing receptor
  • Calcium-sensing receptor (hypocalciuric hypercalcemia 1, severe neonatal hyperparathyroidism)
  • CAR
  • CaSR
  • CASR gene targeted mutation analysis
  • EIG8
  • Extracellular calcium-sensing receptor precursor
  • FHH
  • FIH
  • Genetics
  • GPRC2A
  • Heredity
  • Heritable
  • HHC
  • HHC1
  • HYPOC1
  • Identity or presence
  • Inherited
  • MGC138441
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mut Anl
  • Mutations
  • Nominal
  • NSHPT
  • Parathyroid Cell calcium-sensing receptor
  • PCAR1
  • PCR
  • Point in time
  • Random
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue