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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 09-06-2010 |
Symbol | MMVC |
Location | 18q21.2 |
Name | mirror movements, congenital |
Other name(s) | bimanual synergia |
Corresponding gene | DCC |
Other symbol(s) | CMM |
Genetic determination | autosomal dominant |
Function/system disorder | neurology |
Type | disease |
Remark(s) |