81867-4

LOINC 2.82

NOTCH3 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method

NOTCH3 gene Fam Mut Anl Bld/T

Component

  • NOTCH3 gene mutation analysis limited to known familial mutations

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Find

Scale

  • Doc

Method

  • Molgen

Related names

  • Blood; CADASIL; CASIL; cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy; Document; Fam Mut Anl; Finding; Findings; Genetics; Heredity; Heritable; IMF2; Inherited; LMTED; LTD; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutation; Mutations; Muts; notch 3; Notch homolog 3; PCR; Point in time; Random; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Index terms

  • Blood
  • CADASIL
  • CASIL
  • cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy
  • Document
  • Fam Mut Anl
  • Finding
  • Findings
  • Genetics
  • Heredity
  • Heritable
  • IMF2
  • Inherited
  • LMTED
  • LTD
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mutation
  • Mutations
  • Muts
  • notch 3
  • Notch homolog 3
  • PCR
  • Point in time
  • Random
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue