21730-7

LOINC 2.82

PSAP gene mutations tested for in Blood or Tissue by Molecular genetics method Nominal

PSAP gene Mut Tested Bld/T

Component

  • PSAP gene mutations tested for

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • Blood; COLEC4; Gene mut tested; Genetics; GLBA; Heredity; Heritable; Identity or presence; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Tested; Mutation; Muts; Nominal; PCR; Point in time; Prosaposin; PSAP; PSPA; PSP-A; Random; SAP1; SFTP1; SFTPA1B; SPA; SP-A; SPA1; SP-A1; surfactant protein A1; Tissue; Tissue, unspecified; Variant Gaucher disease; Variant metachromatic leukodystrophy; WB; Whole blood; Whole blood or Tissue

Index terms

  • Blood
  • COLEC4
  • Gene mut tested
  • Genetics
  • GLBA
  • Heredity
  • Heritable
  • Identity or presence
  • Inherited
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mut Tested
  • Mutation
  • Muts
  • Nominal
  • PCR
  • Point in time
  • Prosaposin
  • PSAP
  • PSP-A
  • PSPA
  • Random
  • SAP1
  • SFTP1
  • SFTPA1B
  • SP-A
  • SP-A1
  • SPA
  • SPA1
  • surfactant protein A1
  • Tissue
  • Tissue, unspecified
  • Variant Gaucher disease
  • Variant metachromatic leukodystrophy
  • WB
  • Whole blood
  • Whole blood or Tissue