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GENATLAS PHENOTYPE
last update : 27-06-2023
Symbol NDDOTSA
Location 6q16.1
Name neurodevelopmental delay (NDD), obesity and autism spectrum disorder
Corresponding gene POU3F2
Main clinical features
  • low-to-normal birth weight and infantile feeding difficulties but developed insulin resistance and hyperphagia during childhood
  • while birth and infantile weight records appeared normal, hyperphagia with rapid weight gain was first reported by puberty onset
  • Genetic determination not applicable
    Function/system disorder psychiatry disorder
    Type disease
    Remark(s)