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mirror movements 1
Disease Summary
Associated Targets (1)
Tbio
1
Mondo Description Any familial congenital mirror movements in which the cause of the disease is a mutation in the DCC gene.
Uniprot Description A disorder characterized by contralateral involuntary movements that mirror voluntary ones. While mirror movements are occasionally found in young children, persistence beyond the age of 10 is abnormal. Mirror movements occur more commonly in the upper extremities. Some MRMV1 patients have agenesis of the corpus callosum.
Counts of Target Development Levels for diseases known to be associated with this disease. If the disease has a valid DOID, targets known to be associated with all child diseases are aggregated. Click "Explore Associated Targets" to view more facets and details for the target list.
Description from Mondo Disease Ontology.
Description from UniProt.
DataSources which have contributed target associations to this disease, and the identifiers by which the disease is referenced.
OMIM:157600
MONDO:0008002
High level summary of knowledge for a disease, including descriptions and datasource references.