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General Information
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| Term |
Vissers-Bodmer syndrome |
ID (Ontology) |
DOID:0081397 (Human Disease) |
| Definition |
A syndrome that is characterized by global developmental delay with variably impaired intellectual development, speech delay, motor delay, and behavioral abnormalities apparent from infancy and that has_material_basis_in heterozygous mutation in the CNOT1 gene on chromosome 16q21. |
| 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 | 19 | | 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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Vissers-Bodmer syndrome | 21 | 8 | 1 | ameliorates | Vissers-Bodmer syndrome | 4 | -- | -- | exacerbates | Vissers-Bodmer syndrome | 7 | -- | -- | for disease ribbon | Vissers-Bodmer syndrome | -- | 1 | -- | model of | Vissers-Bodmer syndrome | 10 | 1 | -- |
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Relationships