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General Information
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| Term |
spinocerebellar ataxia type 13 |
ID (Ontology) |
DOID:0050963 (Human Disease) |
| Definition |
An autosomal dominant cerebellar ataxia that is characterized by developmental delay, ataxia, myoclinic jerks, dysarthria, dysphagia and seizure, and has_material_basis_in mutation in the KCNC3 gene. |
| Comment |
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Links to External Ontologies
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DO.org
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Annotations
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Records annotated with this term OR any of its CHILD TERMS
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Records annotated with this exact term (annotations to child terms are NOT included)
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| Data Class | Field | Records |
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| Alleles (FBal) | HUMAN_DISEASE_INTERACTIONS | 1 | | Human Disease Models (FBhh) | DOID | 1 |
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Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
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| Full annotation statements | Relevant FlyBase reports |
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| Alleles | Genes | Human Disease Models |
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spinocerebellar ataxia type 13 | 2 | 3 | 1 | ameliorates | spinocerebellar ataxia type 13 | 1 | -- | -- | for disease ribbon | spinocerebellar ataxia type 13 | -- | 1 | -- | model of | spinocerebellar ataxia type 13 | 1 | 1 | -- |
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Relationships