Conditions and Diseases
Prader–Willi syndrome is a rare genetic disorder in which up to seven genes on chromosome 15 are deleted or unexpressed on the paternal chromosome.
Health: Mental Health: Disorders: Neurodevelopmental: Autism Spectrum
Health: Conditions and Diseases: Nutritional and Metabolic Disorders: Obesity
Health: Conditions and Diseases: Neurological Disorders: Chromosomal
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