Fatal familial insomnia

ICD-11 code : 8E02.2;

Preferred Label : Fatal familial insomnia;

ICD-11 definition : A disease of the brain, caused by inheritance of mutation(s) of normal prion protein genes. This disease is characterized by severe insomnia and autonomic system dysfunction, and is fatal. Confirmation is by pathological examination of the brain and genetic testing.;

ICD-11 synonym : FFI - [fatal familial insomnia];

ICD-11 acronym : FFI;

Details

Origin ID

669154658;

Automatic exact mappings (from CISMeF team)
- Fatal familial insomnia agent (organism) [SNOMED CT concept]
- prion protein [ORDO Gene]
- prion protein (Kanno blood group) [HGNC gene]
Currated CISMeF NLP mapping
- Fatal Familial Insomnia [NCIt concept]
- Fatal familial insomnia [ORDO Disease]
- Fatal familial insomnia [MedDRA Preferred Term]
- Fatal familial insomnia [ICD-9 code]
- Fatal familial insomnia [PASCAL descriptor]
- Fatal familial insomnia [OMIM Phenotype]
- Fatal familial insomnia (disorder) [SNOMED CT concept]
- fatal familial insomnia [DO Concept]
- fatal familial insomnia [SNOMED Notion]
- insomnia, fatal familial [MeSH concept]
- insomnia, fatal familial [MeSH Descriptor]
ICD-10 Mapping
- Atypical virus infection of central nervous system, unspecified [ICD-10 Sub-category]

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