MeSH Browser

MeSH Heading: Insomnia, Fatal Familial
Tree Number(s): C01.207.800.392; C10.228.228.800.392; C10.574.843.512; C10.886.425.800.800.400
Unique ID: D034062
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/D034062
Scope Note: An autosomal dominant disorder characterized by degeneration of the THALAMUS and progressive insomnia. It is caused by a mutation in the prion protein (PRIONS).
Entry Term(s): Familial Fatal Insomnia; Fatal Familial Insomnia; Insomnia Familial Fatal
Previous Indexing: Prion Diseases (1992-2002); Sleep Initiation and Maintenance Disorders (1986-1992)
Public MeSH Note: 2003; see PRION DISEASES 1993-2002
History Note: 2003; use PRION DISEASES 1993-2002
Date Established: 2003/01/01
Date of Entry: 2002/07/03
Revision Date: 2019/06/17

Allowable Qualifiers: blood (BL)

cerebrospinal fluid (CF)

chemically induced (CI)

classification (CL)

complications (CO)

congenital (CN)

diagnosis (DI)

diagnostic imaging (DG)

diet therapy (DH)

drug therapy (DT)

economics (EC)

embryology (EM)

enzymology (EN)

epidemiology (EP)

ethnology (EH)

etiology (ET)

genetics (GE)

history (HI)

immunology (IM)

metabolism (ME)

microbiology (MI)

mortality (MO)

nursing (NU)

parasitology (PS)

pathology (PA)

physiopathology (PP)

prevention & control (PC)

psychology (PX)

radiotherapy (RT)

rehabilitation (RH)

surgery (SU)

therapy (TH)

transmission (TM)

urine (UR)

veterinary (VE)

virology (VI)

Concept UI: M0025976
Scope Note: An autosomal dominant disorder characterized by degeneration of the THALAMUS and progressive insomnia. It is caused by a mutation in the prion protein (PRIONS).
Terms: Insomnia, Fatal Familial Preferred Term
Term UI T051046
Date02/24/1992
LexicalTag NON
ThesaurusID; Fatal Familial Insomnia
Term UI T469715
Date11/13/2001
LexicalTag NON
ThesaurusID; Insomnia Familial Fatal
Term UI T769505
Date04/15/2010
LexicalTag NON
ThesaurusID; Familial Fatal Insomnia
Term UI T769506
Date04/15/2010
LexicalTag NON
ThesaurusID

Insomnia, Fatal Familial MeSH Descriptor Data 2024