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  • Timing is critical for rare diseases. The time patients wait for a diagnosis. The time a clinician spends searching for answers. The time it takes to develop new treatments. What if we could speed that up? We could save lives. We could improve the quality of life for hundreds of millions of people. Every patient has their own story: their own journey, their own symptoms, their own genes, their own face and voice.
Technology now exists to learn from those stories to help recognize these syndromes and find answers faster. We are devoted to using this technology to find answers for you. Every time a patient’s photo and information are analyzed by Face2Gene, our flagship product for clinicians, labs and researchers, the de-identified information “teaches” our system to recognize new syndromes, facial characteristics and genes." ["post_title"]=> string(12) "For Patients" ["post_excerpt"]=> string(0) "" ["post_status"]=> string(7) "publish" ["comment_status"]=> string(6) "closed" ["ping_status"]=> string(6) "closed" ["post_password"]=> string(0) "" ["post_name"]=> string(35) "face2gene-for-rare-disease-patients" ["to_ping"]=> string(0) "" ["pinged"]=> string(0) "" ["post_modified"]=> string(19) "2017-05-15 19:40:29" ["post_modified_gmt"]=> string(19) "2017-05-15 19:40:29" ["post_content_filtered"]=> string(0) "" ["post_parent"]=> int(0) ["guid"]=> string(50) "http://dev-fdna-site.pantheonsite.io/?page_id=2757" ["menu_order"]=> int(0) ["post_type"]=> string(4) "page" ["post_mime_type"]=> string(0) "" ["comment_count"]=> string(1) "0" ["filter"]=> string(3) "raw" }
  • Timing is critical for rare diseases. The time patients wait for a diagnosis. The time a clinician spends searching for answers. The time it takes to develop new treatments. What if we could speed that up? We could save lives. We could improve the quality of life for hundreds of millions of people. Every patient has their own story: their own journey, their own symptoms, their own genes, their own face and voice.

Technology now exists to learn from those stories to help recognize these syndromes and find answers faster. We are devoted to using this technology to find answers for you. Every time a patient’s photo and information are analyzed by Face2Gene, our flagship product for clinicians, labs and researchers, the de-identified information “teaches” our system to recognize new syndromes, facial characteristics and genes.

Help accelerate rare disease advancements. Join the Year of Discovery and ask your doctor to share your story with Face2Gene.

For Patient & Parents
Ask your doctor to include your story

Face2Gene is a suite of phenotyping applications that facilitates comprehensive and precise genetic evaluations. Face2Gene is developed by FDNA and is for use by healthcare professionals. FDNA uses facial analysis, deep learning and artificial intelligence to transform big data into actionable genomic insights to improve and accelerate diagnostics and therapeutics. With the world’s largest network of clinicians, labs and researchers creating one of the fastest growing and most comprehensive genomic databases, FDNA is changing the lives of rare disease patients.

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