Home Page
References OMIM Gene GeneReviews HGMD HGNC
GENATLAS PHENOTYPE
last update : 14-10-2015
Symbol MRD33
Location 7q36.2
Name mental retardation, autosomal dominant 33
Corresponding gene DPP6
Main clinical features
  • microcephaly, severe mental retardation and hyperactivity, short stature
  • Genetic determination autosomal dominant
    Function/system disorder mental retardation
    Type disease
    Remark(s)