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General Information
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| Term |
developmental and epileptic encephalopathy 87 |
ID (Ontology) |
DOID:0112221 (Human Disease) |
| Definition |
A developmental and epileptic encephalopathy characterized by global developmental delay, severely impaired motor and cognitive development, hypotonia, and onset of frequent refractory seizures or infantile spasms between 6 and 15 months of age that has_material_basis_in heterozygous mutation in the CDK19 gene on chromosome 6q21. |
| Also Known As |
"DEE87" ; "early infantile epileptic encephalopathy 87" |
| 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 | 6 | | 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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developmental and epileptic encephalopathy 87 | 6 | 2 | 1 | ameliorates | developmental and epileptic encephalopathy 87 | 1 | -- | -- | for disease ribbon | developmental and epileptic encephalopathy 87 | -- | 1 | -- | model of | developmental and epileptic encephalopathy 87 | 5 | 1 | -- |
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Relationships