Developmental And Epileptic Encephalopathy 48
Disease ID: disease_node_16215
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| Dbxref | MIM:617276 |
|---|---|
| Subclassof | DOID_0050737, DOID_0112202 |
| Data Source | DOID |
| Synonyms | DEE48, early infantile epileptic encephalopathy 48 |
| Doid Label | developmental and epileptic encephalopathy 48 |
| Doid Description | A developmental and epileptic encephalopathy characterized by seizure onset before 1 year of age, global developmental delay, intellectual disability, absent speech, and minimal or absent motor development that has_material_basis_in homozygous or compound heterozygous mutation in the AP3B2 gene on chromosome 15q25. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16215 |
| Doid Id | DOID_0080448 |
| Label | Developmental And Epileptic Encephalopathy 48 |
- 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)