loading...| Preferred Name |
Gerstmann-Straussler disease |
|
| Synonyms |
GSD |
|
| Definitions |
(GSD) - A rare inherited prion disease characterized by adult onset of memory loss, dementia, ataxia, and pathologic deposition of amyloid-like plaques in the brain. GSD presents with progressive limb and truncal ataxia, dysarthria, and cognitive decline in the thirties and forties, and the average disease duration is 7 years. |
|
| ID |
http://identifiers.org/omim/137440 |
|
| altLabel |
GSD |
|
| definition |
(GSD) - A rare inherited prion disease characterized by adult onset of memory loss, dementia, ataxia, and pathologic deposition of amyloid-like plaques in the brain. GSD presents with progressive limb and truncal ataxia, dysarthria, and cognitive decline in the thirties and forties, and the average disease duration is 7 years. |
|
| id |
OMIM:137440 |
|
| notation |
OMIM:137440 |
|
| prefLabel |
Gerstmann-Straussler disease |
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| subClassOf |
| Delete | Mapping To | Ontology | Source |
|---|---|---|---|
| http://identifiers.org/omim/137440 | GEXO | SAME_URI | |
| http://identifiers.org/omim/137440 | RETO | SAME_URI | |
| http://purl.obolibrary.org/obo/OMIM_137440 | CCO | LOOM | |
| http://purl.bioontology.org/ontology/OMIM/137440 | OMIM | LOOM | |
| http://identifiers.org/omim/137440 | GEXO | LOOM | |
| http://identifiers.org/omim/137440 | RETO | LOOM |