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Oligophrenin-1 Syndrome Foundation

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* Disclaimer: RareMDx™ and RareLook™ are not diagnostic but can be regarded as a “hypothetico-deductive method” in the sense that the suggested candidate diseases can be viewed as predictions that require further disease specific testing to confirm a diagnosis. The information, including but not limited to, text, graphics, pages and other material contained on this website are for informational purposes only. The purpose of this website is to promote broad medical/consumer understanding and knowledge about rare diseases. It is not intended to be a substitute for professional medical advice, diagnosis or treatment. Users seeking information about a personal (genetic) disease, syndrome, or condition should always seek the advice of a physician or other qualified health care provider and not delay in seeking it because of something read on this website. Establishing a diagnosis remains the full responsibility of the medical professional.

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