Congenital Mirror Movements

About the Disease
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, cortex and spinal cord, and related phenotypes are easy fatigability and clumsiness

Common Targets
ANXA11 | DNAL4 | APOBEC3D | BAIAP2L2 | RAD51 | NTN1 | DCC | SVEP1

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