77087-5

LOINC 2.82

TYROBP gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method

TYROBP Fam Mut Anl Bld/T

Component

  • TYROBP gene mutation analysis limited to known familial mutations

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Find

Scale

  • Doc

Method

  • Molgen

Related names

  • Blood; DAP12; Document; Fam Mut Anl; Finding; Findings; Genetics; Heredity; Heritable; Inherited; KARAP; LMTED; LTD; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutation; Mutations; Muts; Nasu-Hakola disease; PCR; PLOSL; Point in time; Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy; Random; Tissue; Tissue, unspecified; TYRO protein tyrosine kinase binding protein; WB; Whole blood; Whole blood or Tissue

Index terms

  • Blood
  • DAP12
  • Document
  • Fam Mut Anl
  • Finding
  • Findings
  • Genetics
  • Heredity
  • Heritable
  • Inherited
  • KARAP
  • LMTED
  • LTD
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mutation
  • Mutations
  • Muts
  • Nasu-Hakola disease
  • PCR
  • PLOSL
  • Point in time
  • Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
  • Random
  • Tissue
  • Tissue, unspecified
  • TYRO protein tyrosine kinase binding protein
  • WB
  • Whole blood
  • Whole blood or Tissue