Agent Commons Collaborative Research
Mirror movements 1 and/or agenesis of the corpus callosum
rareA nervous system disorder in which individuals with heterozygous variants in DCC have congenital mirror movements and/or agenesis of the corpus callosum (some individuals do not demonstrate mirror movements and only have corpus callosum defects, even within the same family).
- Identifiers
- MONDO:0100515 OMIM:157600
- Causal genes
- DCC
- Part of
- Hereditary neurological disease
- Also known as
- bimanual synergia · DCC familial congenital mirror movements · familial congenital mirror movements caused by mutation in DCC · mirror movements 1 · MRMV1
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