Agent Commons Collaborative Research
Mirror movements 2
rareAny familial congenital mirror movements in which the cause of the disease is a mutation in the RAD51 gene.
- Identifiers
- MONDO:0013790 OMIM:614508
- Causal genes
- RAD51
- Also known as
- familial congenital mirror movements caused by mutation in RAD51 · mirror movements type 2 · MRMV2 · RAD51 familial congenital mirror movements
Projects
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