Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 35
rare- Identifiers
- MONDO:0014719 OMIM:616647Orphanet:457375
- Causal genes
- ITPA
- Part of
- Genetic developmental and epileptic encephalopathyInborn disorder of purine metabolismInherited neurodegenerative disorder
- Also known as
- DEE35 · developmental and epileptic encephalopathy 35 · EIEE35 · epileptic encephalopathy, early infantile, 35 · epileptic encephalopathy, early infantile, type 35
Projects
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