Concept information
Nervous System Diseases
Central Nervous System Diseases
Central Nervous System Infections
Prion Diseases
...
Sleep Wake Disorders
Dyssomnias
Sleep Disorders, Intrinsic
Sleep Initiation and Maintenance Disorders
Preferred term
Insomnia, Fatal Familial
Type
-
mesh:Descriptor
Definition
- An autosomal dominant disorder characterized by degeneration of the THALAMUS and progressive insomnia. It is caused by a mutation in the prion protein (PRIONS).
Broader concept
Entry terms
- Familial Fatal Insomnia
- Fatal Familial Insomnia
- Insomnia Familial Fatal
Allowable Qualifier(s)
- blood (Qualifier)
- cerebrospinal fluid (Qualifier)
- chemically induced (Qualifier)
- classification (Qualifier)
- complications (Qualifier)
- congenital (Qualifier)
- diagnosis (Qualifier)
- diagnostic imaging (Qualifier)
- diet therapy (Qualifier)
- drug therapy (Qualifier)
- economics (Qualifier)
- embryology (Qualifier)
- enzymology (Qualifier)
- epidemiology (Qualifier)
- ethnology (Qualifier)
- etiology (Qualifier)
- genetics (Qualifier)
- history (Qualifier)
- immunology (Qualifier)
- metabolism (Qualifier)
- microbiology (Qualifier)
- mortality (Qualifier)
- nursing (Qualifier)
- parasitology (Qualifier)
- pathology (Qualifier)
- physiopathology (Qualifier)
- prevention & control (Qualifier)
- psychology (Qualifier)
- radiotherapy (Qualifier)
- rehabilitation (Qualifier)
- surgery (Qualifier)
- therapy (Qualifier)
- transmission (Qualifier)
- urine (Qualifier)
- veterinary (Qualifier)
- virology (Qualifier)
In other languages
-
French
-
IFF (Insomnie Familiale Fatale)
-
Insomnie fatale familiale
URI
http://data.loterre.fr/ark:/67375/JVR-QNF735KF-7
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