/mirror movements 2

mirror movements 2

Rare Disease

MONDO:0013790

Also Known As

RAD51 familial congenital mirror movementsfamilial congenital mirror movements caused by mutation in RAD51mirror movements 2mirror movements type 2MRMV2

Definition

Any familial congenital mirror movements in which the cause of the disease is a mutation in the RAD51 gene.

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Associated Genes

RAD51 ↗

Gene data from MyGene.info • Click to view on NCBI Gene

External Resources

OMIM

OMIM:614508 ↗

GARD

GARD:15814 ↗

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