77050-3

LOINC 2.82

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

SUGCT Fam Mut Anl Bld/T

Component

  • SUGCT gene mutation analysis limited to known familial mutations

Specimen / system

  • Bld/Tiss

Class

  • MOLPATH.MUT

Property

  • Find

Scale

  • Doc

Method

  • Molgen

Related names

  • Blood; C7ORF10; chromosome 7 open reading frame 10; DERP13; Document; Fam Mut Anl; Finding; Findings; FLJ11808; Genetics; glutaric aciduria type III; Heredity; Heritable; Inherited; LMTED; LTD; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mutation; Mutations; Muts; ORF19; PCR; Point in time; Random; Retinitis pigmentosa 54; RP 54; Russel-Silver syndrome; succinyl-CoA:glutarate-CoA transferase; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue

Index terms

  • Blood
  • C7ORF10
  • chromosome 7 open reading frame 10
  • DERP13
  • Document
  • Fam Mut Anl
  • Finding
  • Findings
  • FLJ11808
  • Genetics
  • glutaric aciduria type III
  • Heredity
  • Heritable
  • Inherited
  • LMTED
  • LTD
  • Molecular genetics
  • Molecular pathology
  • MOLPATH
  • MOLPATH.MUTATIONS
  • Mut
  • Mutation
  • Mutations
  • Muts
  • ORF19
  • PCR
  • Point in time
  • Random
  • Retinitis pigmentosa 54
  • RP 54
  • Russel-Silver syndrome
  • succinyl-CoA:glutarate-CoA transferase
  • Tissue
  • Tissue, unspecified
  • WB
  • Whole blood
  • Whole blood or Tissue