Search Ontology:
Human Disease
developmental and epileptic encephalopathy 118
- Term ID
- DOID:0061176
- Synonyms
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- Definition
- A developmental and epileptic encephalopathy characterized by early-onset refractory epilepsy, severe global developmental delay usually with absent speech, hypotonia evolving to spastic quadriparesis, nystagmus, cortical visual impairment, and hematologic abnormalities that has_material_basis_in heterozygous mutation in the TMEM63B gene on chromosome 6p21. https://pubmed.ncbi.nlm.nih.gov/37421948/
- References
- Ontology
- Human Disease ( DOID:0061176 )
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Genes Involved
Zebrafish Models