|
General Information
|
| Term |
familial febrile seizures 11 |
ID (Ontology) |
DOID:0111308 (Human Disease) |
| Definition |
A familial febrile seizures that has_material_basis_in homozygous mutation in the CPA6 gene on chromosome 8p13.2. |
| Also Known As |
"familial febrile convulsions 11" ; "FEB11" |
| Comment |
|
|
Links to External Ontologies
|
|
DO.org
|
|
Annotations
|
|
Records annotated with this term OR any of its CHILD TERMS
|
|
|
|
Records annotated with this exact term (annotations to child terms are NOT included)
|
|
No relevant records available
|
Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
|
| Full annotation statements | Relevant FlyBase reports |
|---|
| Genes |
|---|
familial febrile seizures 11 | 9 | for disease ribbon | familial febrile seizures 11 | 9 | model of | familial febrile seizures 11 | 9 |
|