21763-8LOINC 2.82
HTT gene CAG repeats [Presence] in Blood or Tissue by Molecular genetics method
HTT gene CAG Rpt Bld/T Ql
Definition
- Copy number >36 is considered abnormal and an indication of Huntington disease (HD).
Component
- HTT gene.CAG repeats
Specimen / system
- Bld/Tiss
Class
- MOLPATH.NUCREPEAT
Property
- PrThr
Scale
- Ord
Method
- Molgen
Related names
- 5HTT; 5-HTT; 5-HTTLPR; Blood; Genetics; HD gene; Heredity; Heritable; hSERT; HTT; HTT gene CAG Rpt; huntingtin; Huntington chorea; Huntington disease; Huntington's disease; Inherited; IT15; Molecular genetics; Molecular pathology; MOLPATH; MOLPATH.NUCREPEAT; Neuro; Neurology; OCD1; Ordinal; PCR; Point in time; PR; QL; Qual; Qualitative; Random; Repeat; Screen; 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 CAG Rpt
- HTT gene.CAG repeats
- huntingtin
- Huntington chorea
- Huntington disease
- Huntington's disease
- Inherited
- IT15
- Molecular genetics
- Molecular pathology
- MOLPATH
- MOLPATH.NUCREPEAT
- Neuro
- Neurology
- OCD1
- Ordinal
- PCR
- Point in time
- PR
- QL
- Qual
- Qualitative
- Random
- Repeat
- Screen
- SERT
- SERT1
- solute carrier family 6 (neurotransmitter transporter), member 4
- Tissue
- Tissue, unspecified
3 further terms