Link to this page
Neuroscience Information Framework (NIF) Standard Ontology
Last uploaded:
February 10, 2018
Jump to:
| Id | http://uri.neuinfo.org/nif/nifstd/birnlex_12692
http://uri.neuinfo.org/nif/nifstd/birnlex_12692
|
|---|---|
| Preferred Name | Fatal Familial Insomnia |
| Definitions |
An autosomal dominant disorder characterized by degeneration of the THALAMUS and progressive insomnia. It is caused by a mutation in the prion protein ( PRIONS) (MeSH).
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| 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) (MeSH). |
|---|---|
| preferred label |
Fatal Familial Insomnia
|
| label |
Fatal Familial Insomnia
|
| externalSourceId |
D034062
|
| hasExternalSource | |
| createdDate |
October 5, 2007
|
| 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) (MeSH).
|
| hasCurationStatus | |
| MeshUid |
D034062
|
| subClassOf | |
| hasDefinitionSource | |
| Resource Identifier |
D034062
|
| hasBirnlexCurator | |
| editorial note | |
| type | |
| modifiedDate |
October 5, 2007
|
Add comment
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |