102036-1
LOINC Code
| LOINC code | 102036-1 | |
|---|---|---|
| name | ||
| 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; Abn Prion Prot; abnorm; Bovine spongiform encephalopathy; BSE; Cerebral spinal fluid; Cerebrospinal Fl; Document; Impression; Impression/interpretation of study; Impressions; Interp; Interpretation; Microbiology; Point in time; PR; Prot; PrP; Random; | |
Basic Attributes | ||
| class | MICRO | |
| type | 1 Laboratory | |
| order vs. observation | Abn Prion Prot | |
History/Usage | ||
| first released | ||
| last updated | 2.83 | |
| last change type | MIN - change to field other than name | |
Related Names | ||
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