Developmental And Epileptic Encephalopathy 21
Disease ID: disease_node_16220
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| Dbxref | MIM:615833 |
|---|---|
| Subclassof | DOID_0050737, DOID_0112202 |
| Data Source | DOID |
| Synonyms | DEE21, early infantile epileptic encephalopathy 21 |
| Doid Label | developmental and epileptic encephalopathy 21 |
| Doid Description | A developmental and epileptic encephalopathy characterized by onset in the first months of life by intractable seizures and severely impaired psychomotor development that has_material_basis_in homozygous or compound heterozygous mutation in the NECAP1 gene on chromosome 12p13. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16220 |
| Doid Id | DOID_0080443 |
| Label | Developmental And Epileptic Encephalopathy 21 |
- Outgoing r'ship
SUBCLASS_OFto/from Autosomal Recessive Disease(ID:disease_node_13241) (Disease) - Outgoing r'ship
SUBCLASS_OFto/from Developmental And Epileptic Encephalopathy(ID:disease_node_16165) (Disease)