Abnormal Prion Protein [Interpretation] in Cerebral spinal fluid Document by RT-QuIC 102036-1
LOINC Code
| LOINC code | 102036-1 | ||
|---|---|---|---|
| name | Abnormal Prion Protein [Interpretation] in Cerebral spinal fluid Document by RT-QuIC | ||
| description | Transmissible spongiform encephalopathies (TSEs or prion diseases) are a rare group of invariably fatal neurodegenerative disorders that affect humans and other mammals. TSEs are protein misfolding diseases that involve the accumulation of an abnormally aggregated form of the normal host prion protein (PrP). They are unique among protein misfolding disorders in that they are transmissible and have different strains of infectious agents that are associated with unique phenotypes in vivo. https://pubmed.ncbi.nlm.nih.gov/19157856/#:~:text=Abstract,host%20prion%20protein%20(PrP). | ||
| status | ACTIVE | ||
Fully-Specified Name | |||
| component | Prion protein.abnormal | ||
| property | Imp = Impression/interpretation of study | ||
| time | Pt = Point in time: To identify measures at a point in time. This is a synonym for “spot” or “random” as applied to urine measurements. | ||
| system | CSF = Cerebral spinal fluid | ||
| scale | Doc = Document: A document that could be in many formats (XML, narrative, etc.) | ||
| method | RT-QuIC | ||
Additional Names | |||
| short name | Abn Prion Prot CSF Doc RT-QuIC-Imp | ||
Basic Attributes | |||
| class | MICRO | ||
| type | 1 Laboratory | ||
| order vs. observation | Both | ||
Associated Observations | |||
LOINC codes that represent optional associated observation(s) for a clinical observation or laboratory test. A LOINC term may represent a single associated observation or panel containing several associated observations. | |||
History/Usage | |||
| first released | |||
| last updated | 2.75 | ||
| last change type | ADD - added | ||
Related Names | |||
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