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General Information
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| Term |
cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 2 |
ID (Ontology) |
DOID:0070557 (Human Disease) |
| Definition |
A cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome that has_material_basis_in homozygous mutation in the WDR81 gene on chromosome 17p13.3. |
| Also Known As |
"CAMRQ syndrome 2" ; "CAMRQ2" ; "cerebellar ataxia and mental retardation with or without quadrupedal locomotion 2" (for all, see Synonyms field below) |
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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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No relevant records available
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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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| Genes |
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cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 2 | 1 | for disease ribbon | cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 2 | 1 | model of | cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 2 | 1 |
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