| Descriptor English: | Insomnia, Fatal Familial | ||||||
| Descriptor Spanish: |
Insomnio Familiar Fatal
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| Descriptor Portuguese: | Insônia Familiar Fatal | ||||||
| Descriptor French: | Insomnie familiale fatale | ||||||
| Entry term(s): |
Familial Fatal Insomnia Familial Fatal Insomnias Familial Fatal, Insomnia Familial Fatals, Insomnia Fatal Familial Insomnia Fatal Familial Insomnias Fatal Insomnia, Familial Fatal Insomnias, Familial Fatal, Insomnia Familial Fatals, Insomnia Familial Insomnia Familial Fatal Insomnia Familial Fatals Insomnia, Familial Fatal Insomnias, Familial Fatal Insomnias, Fatal Familial |
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| Tree number(s): |
C01.207.800.392 C10.228.228.800.392 C10.574.843.512 C10.886.425.800.800.400 |
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| RDF Unique Identifier: | https://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). |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy TM transmission UR urine VE veterinary VI virology |
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| Previous Indexing: |
Prion Diseases (1992-2002) Sleep Initiation and Maintenance Disorders (1986-1992) |
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| Public MeSH Note: | 2003; see PRION DISEASES 1993-2002 |
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| History Note: | 2003; use PRION DISEASES 1993-2002 |
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| DeCS ID: | 37279 | ||||||
| Unique ID: | D034062 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 2003/01/01 | ||||||
| Date of Entry: | 2002/07/03 | ||||||
| Revision Date: | 2015/06/22 |
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DISEASES
Infections [C01]Infections
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Insomnia, Fatal Familial
- Preferred
| 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). |
| Preferred term | Insomnia, Fatal Familial |
| Entry term(s) |
Familial Fatal Insomnia Familial Fatal Insomnias Familial Fatal, Insomnia Familial Fatals, Insomnia Fatal Familial Insomnia Fatal Familial Insomnias Fatal Insomnia, Familial Fatal Insomnias, Familial Fatal, Insomnia Familial Fatals, Insomnia Familial Insomnia Familial Fatal Insomnia Familial Fatals Insomnia, Familial Fatal Insomnias, Familial Fatal Insomnias, Fatal Familial |
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