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EpilepsyOntology
Last uploaded:
November 8, 2021
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| Id | http://purl.obolibrary.org/obo/DOID_0050951
http://purl.obolibrary.org/obo/DOID_0050951
|
|---|---|
| Preferred Name | hereditary ataxia |
| Definitions |
A neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements.
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| label |
hereditary ataxia
|
|---|---|
| prefLabel |
hereditary ataxia
|
| database_cross_reference |
GARD:6614
|
| notation |
DOID:0050951
|
| creation_date |
2015-10-05T14:38:17Z
|
| id |
DOID:0050951
|
| created_by |
lschriml
|
| has_obo_namespace |
disease_ontology
|
| 文本定义 |
A neurodegenerative disease that is characterized by slowly progressive incoordination of gait and often associated with poor coordination of hands, speech, and eye movements.
|
| subClassOf | |
| imported from | |
| type |
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