loading...| Preferred Name | obsolete_Gerstmann-Straussler-Scheinker syndrome | |
| Synonyms |
Gerstmann-Straussler-Scheinker disease Subacute spongiform encephalopathy, Gerstmann-Straussler type Gerstmann-Straussler-Scheinker Disease PRION DEMENTIA |
|
| Definitions |
A prion disease characterized by adult onset of memory loss, dementia, ataxia, and pathologic deposition of amyloid-like plaques in the brain. |
|
| ID |
http://www.orpha.net/ORDO/Orphanet_356 |
|
| Obsolete |
true |
|
| database_cross_reference |
MeSH:D016098 OMIM:137440 MedDRA:10072075 UMLS:C0017495 ICD10:A81.8 DOID:4249 |
|
| definition |
A prion disease characterized by adult onset of memory loss, dementia, ataxia, and pathologic deposition of amyloid-like plaques in the brain. |
|
| deprecated |
true |
|
| has_exact_synonym |
Gerstmann-Straussler-Scheinker disease Subacute spongiform encephalopathy, Gerstmann-Straussler type Gerstmann-Straussler-Scheinker Disease PRION DEMENTIA |
|
| label |
obsolete_Gerstmann-Straussler-Scheinker syndrome |
|
| obsoleted_in_version |
3.41.0 |
|
| preferred label |
obsolete_Gerstmann-Straussler-Scheinker syndrome |
|
| prefLabel |
obsolete_Gerstmann-Straussler-Scheinker syndrome |
|
| reason_for_obsolescence |
Replaced with Mondo term. |
|
| term editor |
Sirarat Sarntivijai |
|
| term replaced by | ||
| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://www.orpha.net/ORDO/Orphanet_356 | CCONT | SAME_URI | |
| http://www.orpha.net/ORDO/Orphanet_356 | ORDO | SAME_URI | |
| http://www.orpha.net/ORDO/Orphanet_356 | CCONT | LOOM |