fatal familial insomnia
Information
- Disease name
- fatal familial insomnia
- Disease ID
- DOID:0050433
- Description
- "A prion disease that is characterized by insomnia, hallucinations, dementia and death, located_in the brain." [url:https\://en.wikipedia.org/wiki/Fatal_familial_insomnia]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
- Disase is a (Disease Ontology)
- DOID:649
- Cross Reference ID (Disease Ontology)
- GARD:6429
- Cross Reference ID (Disease Ontology)
- ICD10CM:A81.83
- Cross Reference ID (Disease Ontology)
- ICD9CM:046.72
- Cross Reference ID (Disease Ontology)
- MESH:D034062
- Cross Reference ID (Disease Ontology)
- MIM:600072
- Cross Reference ID (Disease Ontology)
- NCI:C84711
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:83157008
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0206042
- OrphaNumber from OrphaNet (Orphanet)
- 466
- MedGen concept unique identifier (MedGen Concept name)
- C0206042
- MedGen unique identifier (MedGen Concept name)
- 104768