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 C10 Nervous System Diseases D009422 +
  C10.597 Neurologic Manifestations D009461 +
   C10.597.606 Neurobehavioral Manifestations D019954 +
    C10.597.606.643 Mental Retardation D008607 +
     C10.597.606.643.690 Prader-Willi Syndrome D011218 

 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.131 Abnormalities D000013 +
   C16.131.077 Abnormalities, Multiple D000015 +
    C16.131.077.730 Prader-Willi Syndrome D011218 

 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.131 Abnormalities D000013 +
   C16.131.260 Chromosome Disorders D025063 +
    C16.131.260.700 Prader-Willi Syndrome D011218 

 C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities D009358 +
  C16.320 Genetic Diseases, Inborn D030342 +
   C16.320.180 Chromosome Disorders D025063 +
    C16.320.180.700 Prader-Willi Syndrome D011218 

 C18 Nutritional and Metabolic Diseases D009750 +
  C18.654 Nutrition Disorders D009748 +
   C18.654.726 Overnutrition D044343 +
    C18.654.726.500 Obesity D009765 +
     C18.654.726.500.740 Prader-Willi Syndrome D011218