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GENATLAS PHENOTYPE
last update : 15-06-2011
Symbol OCGA
Location 9q34.13
Name bilateral occipital cortical gyration abnormalities
Corresponding gene LAMC3
Main clinical features
  • unusual occipital malformation, PMID: 21572413
  • occipital cortical malformations characterized by complex gyration abnormalities
  • Genetic determination autosomal recessive
    Function/system disorder neurology
    Type malformation
    Mechanism(s)
    Gene mutationChromosome rearrangementEffectComments
    various types      
    Remark(s)