Insomnia, Fatal Familial [insomnie fatální familiární]
topical
10
- Terms
-
fatální familiární insomnie
-
Familial Fatal Insomnia
Fatal Familial Insomnia
Insomnia Familial Fatal
Persistent link
https://www.medvik.cz/link/D034062
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).
- DUI
- D034062 MeSH Browser
- CUI
- M0025976
- Previous indexing
- Prion Diseases (1992-2002); Sleep Initiation and Maintenance Disorders (1986-1992)
- History note
- 2003; use PRION DISEASES 1993-2002
- Public note
- 2003; see PRION DISEASES 1993-2002
Allowable subheadings
- BL
- blood
- CF
- cerebrospinal fluid
- CI
- chemically induced
- CL
- classification 1
- CO
- complications
- CN
- congenital
- DI
- diagnosis 3
- DG
- diagnostic imaging
- DH
- diet therapy
- DT
- drug therapy
- EC
- economics
- EM
- embryology
- EN
- enzymology
- EP
- epidemiology
- EH
- ethnology
- ET
- etiology 3
- GE
- genetics 2
- HI
- history
- IM
- immunology
- ME
- metabolism
- MI
- microbiology
- MO
- mortality
- NU
- nursing
- PS
- parasitology
- PA
- pathology
- PP
- physiopathology 1
- PC
- prevention & control
- PX
- psychology
- RT
- radiotherapy
- RH
- rehabilitation
- SU
- surgery
- TH
- therapy 2
- TM
- transmission
- UR
- urine
- VE
- veterinary
- VI
- virology
...
Occurrences in Medvik records
C
Diseases