75386-3

LOINC 2.82

MEN1 gene mutation analysis limited to known familial mutations in Blood or Tissue by Molecular genetics method

MEN1 gene Fam Mut Anl Bld/T

Component

  • MEN1 gene mutation analysis limited to known familial mutations

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Find

Scale

  • Doc

Method

  • Molgen

Related names

  • Blood; Document; Fam Mut Anl; Finding; Findings; Genetics; Heredity; Heritable; Inherited; LMTED; LTD; MEAI; Menin; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; multiple endocrine neoplasia I; Multiple endocrine neoplasia type I; Mut; Mutation; Mutations; Muts; PCR; Point in time; Random; SCG2; Tissue; Tissue, unspecified; WB; Wermer syndrome; Whole blood; Whole blood or Tissue; Zollinger-Ellison syndrome

Index terms

  • Blood
  • Document
  • Fam Mut Anl
  • Finding
  • Findings
  • Genetics
  • Heredity
  • Heritable
  • Inherited
  • LMTED
  • LTD
  • MEAI
  • Menin
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • multiple endocrine neoplasia I
  • Multiple endocrine neoplasia type I
  • Mut
  • Mutation
  • Mutations
  • Muts
  • PCR
  • Point in time
  • Random
  • SCG2
  • Tissue
  • Tissue, unspecified
  • WB
  • Wermer syndrome
  • Whole blood
  • Whole blood or Tissue
  • Zollinger-Ellison syndrome