Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 23
rare- Identifiers
- MONDO:0014371 OMIM:615859Orphanet:411986
- Causal genes
- DOCK7
- Part of
- Congenital nervous system disorderGenetic developmental and epileptic encephalopathyMonogenic epilepsyMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- developmental and epileptic encephalopathy 23 · early-onset epileptic encephalopathy-cortical blindness-intellectual disability-facial dysmorphism syndrome · EIEE23 · epilepsy-cortical blindness-intellectual disability-facial dysmorphism syndrome · epileptic encephalopathy, early infantile, 23
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