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MIRAGE
developmental and epileptic encephalopathy 31B
Summary
- Synonym
-
- DEE31B
- Definition
- A developmental and epileptic encephalopathy characterized by early-onset epilepsy, generalized muscular hypotonia, visual impairment, and severe neurodevelopmental delay that has_material_basis_in homozygous mutation in the DNM1 gene on chromosome 9q34.
- Super Class
- autosomal recessive disease developmental and epileptic encephalopathy
External Links
- Disease Ontology
- DOID:0070376
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001508 | Failure to thrive |
| HP:0012704 | Widened subarachnoid space |
| HP:0000648 | Optic atrophy |
| HP:0004305 | Involuntary movements |
| HP:0000341 | Narrow forehead |
| HP:0002179 | Opisthotonus |
| HP:0011344 | Severe global developmental delay |
| HP:0001274 | Agenesis of corpus callosum |
| HP:0000212 | Gingival overgrowth |
| HP:0002119 | Ventriculomegaly |
