Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 73
rare- Identifiers
- MONDO:0034106 OMIM:618379Orphanet:544503
- Causal genes
- RNF13
- Part of
- Congenital nervous system disorderGenetic developmental and epileptic encephalopathyMonogenic epilepsyMultiple congenital anomalies/dysmorphic syndrome-intellectual disability
- Also known as
- DEE73 · developmental and epileptic encephalopathy 73 · epileptic encephalopathy, early infantile, 73 · rnf13-related severe early-onset epileptic encephalopathy
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