34718-7

LOINC 2.82

CFTR gene mutations found [Identifier] in Amniotic fluid by Molecular genetics method Nominal

CFTR Mut Anl Amn

Component

  • CFTR gene targeted mutation analysis

Specimen / system

  • Amnio fld

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • ABC35; ABCC7; AF; Amn; Amn fl; Amnio; Amniotic flu; Amniotic fluid; CBAVD; CF; CFA; CFTR/MRP; Cystic fibrosis transmembrane conductance regulator; cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7); dJ760C5.1; Genetics; Gyn; Gynecology; Heredity; Heritable; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; MRP7; Mut; Mut Anl; Mutations; Nominal; OB; ObGyn; Obstetrics; PCR; Point in time; Random; TNR-CFTR

Index terms

  • ABC35
  • ABCC7
  • AF
  • Amn
  • Amn fl
  • Amnio
  • Amniotic flu
  • Amniotic fluid
  • CBAVD
  • CF
  • CFA
  • CFTR gene targeted mutation analysis
  • CFTR/MRP
  • Cystic fibrosis transmembrane conductance regulator
  • cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
  • dJ760C5.1
  • Genetics
  • Gyn
  • Gynecology
  • Heredity
  • Heritable
  • Identity or presence
  • Inherited
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • MRP7
  • Mut
  • Mut Anl
  • Mutations
  • Nominal
  • OB
  • ObGyn
  • Obstetrics
  • PCR
  • Point in time
  • Random
  • TNR-CFTR