Developmental And Epileptic Encephalopathy 37
Disease ID: disease_node_16228
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| Dbxref | MIM:616981 |
|---|---|
| Subclassof | DOID_0050737, DOID_0112202 |
| Data Source | DOID |
| Synonyms | DEE37, early infantile epileptic encephalopathy 37 |
| Doid Label | developmental and epileptic encephalopathy 37 |
| Doid Description | A developmental and epileptic encephalopathy characterized by onset of intractable seizures or abnormal movement in the first years of life and developmental delay or regression after seizure onset that has_material_basis_in homozygous or compound heterozygous mutation in the FRRS1L gene (604574) on chromosome 9q31. |
| Has Material Basis In | GENO_0000148 |
| Disease Node Id | disease_node_16228 |
| Doid Id | DOID_0080435 |
| Label | Developmental And Epileptic Encephalopathy 37 |
- 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)