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GENATLAS PHENOTYPE
last update : 04-11-2015
Symbol MYMY5
Location 10q23.31
Name Moyamoya disease susceptibility 5
Corresponding gene ACTA2
Main clinical features
  • bilateral stenosis and/or occlusion of the terminal portion of the internal carotid artery, presenting in young patients with transient motor disturbances and in adult with intracranial hemorrhage
  • Genetic determination autosomal dominant
    Function/system disorder cardiovascular
    neurology
    Type disease
    Remark(s)