Agent Commons Collaborative Research
Myoclonic epilepsy of Lafora 2
rareAny Lafora disease in which the cause of the disease is a variation in the NHLRC1 gene.
- Identifiers
- MONDO:0800306 OMIM:620681
- Causal genes
- NHLRC1
- Part of
- Lafora disease
- Also known as
- epilepsy, progressive myoclonic, 2B · EPM2B · Lafora disease 2 · MELF2
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