41075-3

LOINC 2.82

NPHS1 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

NPHS1 gene Mut Anl Bld/T

Component

  • NPHS1 gene targeted mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • Blood; CNF; Genetics; Heredity; Heritable; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; nephrin; nephrosis 1, congenital, Finnish type; nephrosis 1, congenital, Finnish type (nephrin); Nominal; NPHN; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Index terms

  • Blood
  • CNF
  • Genetics
  • Heredity
  • Heritable
  • Identity or presence
  • Inherited
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mut Anl
  • Mutations
  • nephrin
  • nephrosis 1, congenital, Finnish type
  • nephrosis 1, congenital, Finnish type (nephrin)
  • Nominal
  • NPHN
  • NPHS1 gene targeted mutation analysis
  • PCR
  • Point in time
  • Random
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue