fatal insomnia
Prion disease of the human brain
Facts
15 properties- Instance of
- class of disease, symptom or sign[2]
- Subclass of
- rare disease, inherited prion disease, genetic disease, thalamic disease, transmissible spongiform encephalopathy, insomnia[3][4][5][6][7][8]
- Short name
- FFI[23]
- Age of onset
- adult onset[28]
- Has phenotype
- dementia, Primary autonomic failure, depression, hallucination, anxiety, arterial hypertension, dysarthria, tachycardia, dysphagia, basal ganglia disease, Sleep-wake cycle disturbance, excessive tearing, sleep apnea, Short term memory impairment, Reduced attention regulation, diplopia, weight loss, fever, constipation, Loss of speech, adrenal gland hyperfunction[30][31][32][33][34][35][36][37][38][39][40][41][42][43]
- Health specialty
- psychiatry, sleep medicine, neuropathology[24][25][26]
- ICD-9-CM
- 046.72[21]
- ICPC 2 ID
- N73[9]
- NCI Thesaurus ID
- C84711[22]
- On focus list of Wikimedia project
- WikiProject Medicine[29]
- P14541
- 13u6Aj
- P14914
- D00466
- Prevalence
- +0.000001[20]
🏷️ Also known as
en fatal familial insomnia
en Familial fatal insomnia
en Insomnia, Fatal Familial
en Insomnia familial fatal
en FFI
en Fatal insomnia
ar أرق مميت
ar أرق وراثي مميت
cs Fatální familiární insomnie
da Dødelig søvnløshed
de Tödliche familiäre Schlaflosigkeit
de Letale familiäre Insomnie
de Familiäre fatale Insomnie
el Θανάσιμη αϋπνία
es Insomnio letal
es insomnio familiar fatal
es Insomnio familiar letal
es Insomnio fatal
fa بیخوابی خانوادگی مرگآور
fi fataali familiaalinen insomnia
🔖 Identifiers · 31
- OpenAlex ID
- C2779455247
- Image (Wikimedia Commons)
- Cranial imaging of a FFI patient.jpg ↗
- Archive of Our Own tag
- Fatal familial insomnia
- BabelNet ID
- 03189477n
- Bibliothèque nationale de France ID
- 13549188z
- Disease Ontology ID
- DOID:0050433
- DiseasesDB
- 32177
- Encyclopedia of China (Third Edition) ID
- 133490
- Exact match
- purl.obolibrary.org, identifiers.org, www.orpha.net
- Freebase ID
- /m/0b_bf
- GARD rare disease ID
- 6429
- GeneReviews ID
- NBK1229
Show all 31 identifiers +19
- ICD-10 ID
- A81.981.9
- ICD-11 ID (Foundation)
- 669154658
- ICD-11 ID (MMS)
- 8E02.2
- ICD-9 ID
- 046.8046.8
- KBpedia ID
- FatalFamilialInsomnia
- MeSH descriptor ID
- D034062
- MeSH tree code
- C10.228.228.800.392, C10.574.843.512, C10.886.425.800.800.400, C01.207.800.392
- Microsoft Academic ID (discontinued)
- 2779455247
- Mondo ID
- MONDO_0010808
- OMIM ID
- 600072
- Orphanet ID
- 466
- Pschyrembel Online ID
- tödliche familiäre Insomnie
- Quora topic ID
- Fatal-Familial-Insomnia
- SNOMED CT ID
- 83157008
- Subreddit
- fatalfamilialinsomnia
- UMLS CUI
- C0206042
- UniProt disease ID
- DI-01607
- WikiProjectMed ID
- Fatal insomnia
🔗 Connections
Symptoms and signs 9
fever,
arterial hypertension,
dementia,
insomnia,
hallucination,
phobia,
ageing,
panic attack
+1 more
Subclass of 5
Health specialty 3
Genetic association 1
Instance of 1
On focus list of Wikimedia project 1
← Genetic association 1
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Summary
fatal insomnia is a class of disease[1].