42321-0LOINC 2.82
HTT gene mutations found [Identifier] in Blood or Tissue by Molecular genetics method Nominal
HTT gene Mut Anl Bld/T
Component
- HTT gene targeted mutation analysis
Specimen / system
- Bld/Tiss
Class
- MOLPATH.MUT
Property
- Prid
Scale
- Nom
Method
- Molgen
Related names
- 5HTT; 5-HTT; 5-HTTLPR; Blood; Genetics; HD gene; Heredity; Heritable; hSERT; HTT; huntingtin; Huntington chorea; Huntington disease; Huntington's disease; Identity or presence; Inherited; IT15; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.MUTATIONS; Mut; Mut Anl; Mutations; Nominal; OCD1; PCR; Point in time; Random; SERT; SERT1; solute carrier family 6 (neurotransmitter transporter), member 4; Tissue; Tissue, unspecified; WB; Whole blood; Whole blood or Tissue
Index terms
- 5-HTT
- 5-HTTLPR
- 5HTT
- Blood
- Genetics
- HD gene
- Heredity
- Heritable
- hSERT
- HTT
- HTT gene targeted mutation analysis
- huntingtin
- Huntington chorea
- Huntington disease
- Huntington's disease
- Identity or presence
- Inherited
- IT15
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.MUTATIONS
- Mut
- Mut Anl
- Mutations
- Nominal
- OCD1
- PCR
- Point in time
- Random
- SERT
- SERT1
- solute carrier family 6 (neurotransmitter transporter), member 4
- Tissue
- Tissue, unspecified
- WB
- Whole blood
- Whole blood or Tissue