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GENATLAS PHENOTYPE
last update : 16-05-2018
Symbol FECD9
Location 18q21.1
Name corneal dystrophy, Fuchs endothelial 9
Corresponding gene LOXHD1
Main clinical features
  • late-onset corneal dystrophy,
  • degenerative genetic disorder of the corneal endothelium, late-onset
  • Genetic determination autosomal dominant
    Function/system disorder eye
    Type disease
    Remark(s)