Details of Disease

General Information of Disease (ID: DISXVLIN)

Disease Name Mirror movements 2
Synonyms MRMV2; mirror movements 2; familial congenital mirror movements caused by mutation in RAD51; mirror movements type 2; RAD51 familial congenital mirror movements
Definition Any familial congenital mirror movements in which the cause of the disease is a mutation in the RAD51 gene.
Disease Hierarchy
DISJLV92: Familial congenital mirror movements
DISXVLIN: Mirror movements 2
Disease Identifiers
MONDO ID
MONDO_0013790
UMLS CUI
C3281089
OMIM ID
614508
MedGen ID
482719

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 2 DTT Molecule(s)
Gene Name DTT ID Evidence Level Mode of Inheritance REF
RAD51 TTC0G1L Strong Autosomal dominant [1]
RAD51 TTC0G1L Strong Biomarker [2]
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This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
RAD51 OTNVWGC1 Strong Autosomal dominant [1]
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References

1 RAD51 haploinsufficiency causes congenital mirror movements in humans. Am J Hum Genet. 2012 Feb 10;90(2):301-7. doi: 10.1016/j.ajhg.2011.12.002. Epub 2012 Feb 2.
2 A novel DCC mutation and genetic heterogeneity in congenital mirror movements. Neurology. 2011 Jan 18;76(3):260-4. doi: 10.1212/WNL.0b013e318207b1e0.