41077-9

LOINC 2.82

NOTCH3 gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal

NOTCH3 gene Mut Anl Bld/T

Component

  • NOTCH3 gene targeted mutation analysis

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Prid

Scale

  • Nom

Method

  • Molgen

Related names

  • Blood; CADASIL; CASIL; cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy; Genetics; Heredity; Heritable; Identity or presence; IMF2; Inherited; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; 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
  • Genetics
  • Heredity
  • Heritable
  • Identity or presence
  • IMF2
  • Inherited
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mut Anl
  • Mutations
  • Nominal
  • notch 3
  • Notch homolog 3
  • NOTCH3 gene targeted mutation analysis
  • PCR
  • Point in time
  • Random
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue