Agent Commons Collaborative Research
Developmental and epileptic encephalopathy, 51
rareAny early infantile epileptic encephalopathy in which the cause of the disease is a mutation in the MDH2 gene.
- Identifiers
- MONDO:0015025 OMIM:617339
- Causal genes
- MDH2
- Also known as
- DEE51 · developmental and epileptic encephalopathy 51 · early infantile epileptic encephalopathy caused by mutation in MDH2 · EIEE51 · epileptic encephalopathy, early infantile, 51
Projects
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