Gerstmann-Straussler-Scheinker syndrome

ICD-11 code : 8E02.1;

Preferred Label : Gerstmann-Straussler-Scheinker syndrome;

ICD-11 definition : A disease caused by inheritance of mutation(s) in normal prion protein genes. This disease is characterized by cerebellar ataxia, decreased coordination, dysmetria, or dysarthria, and is fatal. Confirmation is by pathological examination of the brain and genetic testing.;

Details

Origin ID

406818835;

Automatic exact mappings (from CISMeF team)
- Gerstmann-Straussler-Scheinker syndrome [DO Concept]
Currated CISMeF NLP mapping
- Gerstmann Straussler Scheinker disease [Disease (Nov.)]
- Gerstmann Straussler Scheinker syndrome [MedDRA Preferred Term]
- Gerstmann-Straeussler-Scheinker syndrome [MedDRA LLT]
- Gerstmann-Straussler-Scheinker Disease [NCIt concept]
- Gerstmann-Straussler-Scheinker disease [MeSH concept]
- Gerstmann-Straussler-Scheinker syndrome [ORDO Disease]
- Gerstmann-Straussler-Scheinker syndrome (disorder) [SNOMED CT concept]
- Gerstmann-Sträussler-Scheinker syndrome [PASCAL descriptor]
- Gerstmann-straussler disease [OMIM Phenotype]
- gerstmann-straussler-scheinker disease [MeSH Descriptor]
- gerstmann-straussler-scheinker syndrome [SNOMED Notion]
ICD-10 Mapping
- Atypical virus infection of central nervous system, unspecified [ICD-10 Sub-category]

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