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loading...| Preferred Name | Insomnia, Fatal Familial [Disease/Finding] | |
| Synonyms |
Familial Fatal Insomnia Fatal Familial Insomnia Insomnia Familial Fatal Insomnia, Fatal Familial |
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| ID |
http://purl.bioontology.org/ontology/NDFRT/N0000011042 |
|
| altLabel |
Familial Fatal Insomnia Fatal Familial Insomnia Insomnia Familial Fatal Insomnia, Fatal Familial |
|
| cui |
C0206042 |
|
| MESH 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). |
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| MESH DUI |
D034062 |
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| MeSH name |
Insomnia, Fatal Familial |
|
| MESH UI |
M0025976 |
|
| NDFRT kind |
DISEASE_KIND |
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| notation |
N0000011042 |
|
| NUI |
N0000011042 |
|
| prefLabel |
Insomnia, Fatal Familial [Disease/Finding] |
|
| SNOMED CID |
83157008 |
|
| tui |
T047 |
|
| subClassOf |
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