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ENMirror Movements 1 (MRMV1)
Alias:
Congenital Mirror Movement Disorder
Mirror Movements 1 and/or Agenesis of the Corpus Callosum
Hereditary Congenital Controlateral Synkinesia
Familial Congenital Controlateral Synkinesia
Isolated Congenital Controlateral Synkinesia
Hereditary Congenital Mirror Movements
Familial Congenital Mirror Movements
Isolated Congenital Mirror Movements
Congenital Mirror Movements
Bimanual Synergia
Mirror Movements, Congenital
Mirror Movements
Mrmv1
Mirror Movements, Type 1
Bimanual Synkinesis
Cmm
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Mirror Movements 1, also known as congenital mirror movement disorder, is related to klippel-feil syndrome and melanoma. An important gene associated with Mirror Movements 1 is DCC (DCC Netrin 1 Receptor), and among its related pathways/superpathways is Regulation of commissural axon pathfinding by SLIT and ROBO. Affiliated tissues include brain and cortex, and related phenotypes are abnormality of movement and easy fatigability
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