Developmental And Epileptic Encephalopathy 38
Disease ID: disease_node_16188
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| Dbxref | MIM:617020 |
|---|---|
| Subclassof | DOID_0050737, DOID_0112202 |
| Data Source | DOID |
| Synonyms | DEE38, early infantile epileptic encephalopathy 38 |
| Doid Label | developmental and epileptic encephalopathy 38 |
| Doid Description | A developmental and epileptic encephalopathy characterized by onset of seizures between 4 and 7 months of age, severely impaired global development, hypotonia with poor head control, and visual inattention that has_material_basis_in homozygous or compound heterozygous mutation in the ARV1 gene on chromosome 1q42. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16188 |
| Doid Id | DOID_0080417 |
| Label | Developmental And Epileptic Encephalopathy 38 |
- 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)