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General Information
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| Term |
Coffin-Siris syndrome 6 |
ID (Ontology) |
DOID:0080297 (Human Disease) |
| Definition |
A Coffin-Siris syndrome that is characterized by short stature, sparse hair, mild to severe intellectual disability, coarse facial features, and variable behavioral anomalies and that has_material_basis_in heterozygous mutation in the ARID2 gene on chromosome 12q12. |
| 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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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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Coffin-Siris syndrome 6 | 1 | for disease ribbon | Coffin-Siris syndrome 6 | 1 | model of | Coffin-Siris syndrome 6 | 1 |
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