Details of Disease

General Information of Disease (ID: DISGKNLN)

Disease Name Mirror movements 1
Synonyms
MRMV1; mirror movements, congenital; bimanual synergia; mirror movements 1 and/Or agenesis of the corpus callosum; mirror movements 1; DCC familial congenital mirror movements; mirror movements type 1; familial congenital mirror movements caused by mutation in DCC
Definition Any familial congenital mirror movements in which the cause of the disease is a mutation in the DCC gene.
Disease Hierarchy
DISJLV92: Familial congenital mirror movements
DISJ95WV: Mirror movements 1 and/or agenesis of the corpus callosum
DISGKNLN: Mirror movements 1
Disease Identifiers
MONDO ID
MONDO_0008002
UMLS CUI
C1834870
OMIM ID
157600
MedGen ID
320461

Molecular Interaction Atlas (MIA) of This Disease

Molecular Interaction Atlas (MIA)
This Disease Is Related to 1 DOT Molecule(s)
Gene Name DOT ID Evidence Level Mode of Inheritance REF
DCC OT2C1SHW Definitive Autosomal dominant [1]
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References

1 Familial congenital mirror movements: report of a large 4-generation family. Neurology. 2009 Sep 1;73(9):729-31. doi: 10.1212/WNL.0b013e3181b59bda.