94225-0LOINC 2.82
TTR gene full mutation analysis in Blood or Tissue by Sequencing
TTR gene Full Mut Anl Bld/T Seq
Definition
- Full gene sequence analysis, including all coding regions and intron/exon boundaries, of the TTR gene for the diagnosis of transthyretin-associated familial amyloidosis, the most common hereditary amyloidosis.
Component
- TTR gene full mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH
Property
- Find
Scale
- Doc
Method
- Sequencing
Related names
- Blood; CTS; CTS1; Document; Finding; Findings; full gene sequencing; Full Mut Anl; Genetics; HEL111; Heredity; Heritable; high-throughput sequencing; HsT2651; HTS; Inherited; Molecular pathology; MOLPATH; Mut; Mutations; Next generation sequencing; NGS; PALB; Point in time; Random; sequencing of entire coding region; TBPA; Tissue; Tissue, unspecified; transthyretin; Transthyretin (prealbumin, amyloidosis type I) gene; WB; Whole blood; Whole blood or Tissue
Index terms
- Blood
- CTS
- CTS1
- Document
- Finding
- Findings
- full gene sequencing
- Full Mut Anl
- Genetics
- HEL111
- Heredity
- Heritable
- high-throughput sequencing
- HsT2651
- HTS
- Inherited
- Molecular pathology
- MOLPATH
- Mut
- Mutations
- Next generation sequencing
- NGS
- PALB
- Point in time
- Random
- sequencing of entire coding region
- TBPA
- Tissue
- Tissue, unspecified
- transthyretin
- Transthyretin (prealbumin, amyloidosis type I) gene
- WB
- Whole blood
- Whole blood or Tissue