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developmental and epileptic encephalopathy 89
Summary
- Synonym
-
- DEE89
- early infantile epileptic encephalopathy 89
- Definition
- A developmental and epileptic encephalopathy characterized by onset in the first days or months of life of seizures, profound global developmental delay with impaired intellectual development, absent speech, axial hypotonia, and spastic quadriparesis that has_material_basis_in homozygous or compound heterozygous mutation in the GAD1 gene on chromosome 2q31.1.
- Super Class
- autosomal recessive disease developmental and epileptic encephalopathy
External Links
- Disease Ontology
- DOID:0112223
- Mondo Disease Ontology
- OMIM
Related Genes
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002079 | Hypoplasia of the corpus callosum |
| HP:0002187 | Intellectual disability, profound |
| HP:0002273 | Tetraparesis |
| HP:0002487 | Hyperkinetic movements |
| HP:0002553 | Highly arched eyebrow |
| HP:0002650 | Scoliosis |
| HP:0003593 | Infantile onset |
| HP:0003623 | Neonatal onset |
| HP:0003811 | Neonatal death |
| HP:0003819 | Death in childhood |
