Statements (28)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
gptkb:disease
genetic disorder prion disease |
| gptkbp:diagnosedBy |
neurological examination
genetic testing |
| gptkbp:firstDescribed |
1936
|
| gptkbp:frequency |
rare
|
| gptkbp:fullName |
gptkb:Gerstmann–Sträussler–Scheinker_syndrome
|
| https://www.w3.org/2000/01/rdf-schema#label |
GSS syndrome
|
| gptkbp:ICD-10_code |
A81.8
|
| gptkbp:inheritance |
autosomal dominant
|
| gptkbp:mutationAssociatedWith |
gptkb:PRNP_gene
|
| gptkbp:namedAfter |
gptkb:Ilya_Scheinker
gptkb:Josef_Gerstmann gptkb:Ernst_Sträussler |
| gptkbp:OMIM |
137440
|
| gptkbp:onset |
adult
|
| gptkbp:prognosis |
progressive and fatal
|
| gptkbp:relatedTo |
gptkb:Creutzfeldt–Jakob_disease
gptkb:fatal_familial_insomnia |
| gptkbp:symptom |
gptkb:dementia
ataxia extrapyramidal signs progressive cerebellar ataxia pyramidal signs |
| gptkbp:treatment |
supportive care
|
| gptkbp:bfsParent |
gptkb:Gerstmann–Sträussler–Scheinker_syndrome
|
| gptkbp:bfsLayer |
7
|