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The Genesis Foundation For Children | More Than Medical Care
The Genesis Foundation for Children diagnoses, treats and provide coordinated care for children with rare diseases and genetic disorders.
Sarepta Therapeutics | Biopharmaceutical Company for Rare Diseases
We are focused on the development of precision genetic medicines to treat rare neuromuscular and central nervous system diseases. Learn more about Sarepta.
Sarepta Therapeutics | Biopharmaceutical Company for Rare Diseases
We are focused on the development of precision genetic medicines to treat rare neuromuscular and central nervous system diseases. Learn more about Sarepta.
Sarepta Therapeutics | Biopharmaceutical Company for Rare Diseases
We are focused on the development of precision genetic medicines to treat rare neuromuscular and central nervous system diseases. Learn more about Sarepta.
knowHAE | Get to know hereditary angioedema (HAE)
Learn more about the rare disease hereditary angioedema (HAE), including signs and symptoms, how it’s diagnosed, treatment options, and more.
knowHAE | Iepazīt hereditāra angioedema (HAE)
Learn more about the rare disease hereditary angioedema (HAE), including signs and symptoms, how it’s diagnosed, treatment options, and more.
Introduction to Rare Genetic Disorders of Obesity
In rare instances, a rare genetic disorder of obesity can stop your brain from understanding when your body is full. Learn how this can happen.
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Learn about how Shockwave Medical is changing the landscape of how calcified cardiovascular disease is treated with Intravascular Lithotrispy (IVL).
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Rare and genetic disease publisher and learning platform.
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Cure Rare Disease
Cure Rare Disease™ is developing customized therapeutics for those who have been diagnosed with rare, genetic diseases that have no treatment or cures. Through partnerships and collaboration, our world-renowned researchers build life-saving therapeutics that are custom to the patient they are made to treat.
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BioMarin is a world leader in developing and commercializing innovative biopharmaceuticals for rare diseases driven by genetic causes.
3billion | Genetic test for rare disease patients
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Rare Genetic Obesity: Causes, Signs, Diagnosis - Uncommon Obesity
Learn more about rare genetic disorders of obesity, including dysfunction in a key pathway involved in hunger regulation, symptoms to look for, and options for diagnosis.
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Home | On Route
Beating autoimmune disease ! Are you living with chronic illness? Are you sick of being sick? Perhaps you are diagnosed with an utoimmune disease? You can overcome autoimmune disease. You can beat autoimmune disease. You can arrest autoimmune disease. Learn how to beat autoimmune disease. After battling with autoimmune disease, I did extentisve reasech and cam eaccross functional medicine. They treat the root cause. By treating the root cause of autoimmune disease you can beat autoimmune disease. Treating symptoms is not the answer. I will teach you how.
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Learn about spinal muscular atrophy (SMA), a neuromuscular disease, and how a genetic test for SMA is performed to confirm diagnosis.
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Learn about spinal muscular atrophy (SMA), a neuromuscular disease, and how a genetic test for SMA is performed to confirm diagnosis.
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Learn about spinal muscular atrophy (SMA), a neuromuscular disease, and how a genetic test for SMA is performed to confirm diagnosis.
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Learn about spinal muscular atrophy (SMA), a neuromuscular disease, and how a genetic test for SMA is performed to confirm diagnosis.
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Learn about spinal muscular atrophy (SMA), a neuromuscular disease, and how a genetic test for SMA is performed to confirm diagnosis.
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What is Gaucher disease? Visit GaucherDisease.info
Visit GaucherDisease.info to learn about the rare genetic disorder, Gaucher disease (or Gaucher’s). Symptoms include enlarged liver and spleen, bleeding and bruising, and joint pain.
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What is Gaucher disease? Visit GaucherDisease.info
Visit GaucherDisease.info to learn about the rare genetic disorder, Gaucher disease (or Gaucher’s). Symptoms include enlarged liver and spleen, bleeding and bruising, and joint pain.
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Home | Arena Pharmaceuticals (en-US)
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Learn About Fabry Disease Inheritance | Fabry Disease Family Tree
Learn about Fabry disease inheritance and genetics. Create your Fabry Family Tree.
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Changing the perception of obesity and redefining how it is treated Together, we can bring a new perspective that treatspeople as more than pounds on a scale, addressingthe root causes of obesity with the best inmedical science, behavioral tools and psychology.Because obesity is not a lifestyle issue. It’s not a lackof willpower or some personal … HOME Read More »
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National Gaucher Foundation | Gaucher Disease - Symptoms, Treatment, & Education
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Infinity BiologiX aims to understand the genetic causes of common, complex diseases and to discover diagnoses, treatments and, eventually, cures for these
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Latest news Read FIN’s latest updates, upcoming events and all news relating to Fabry Disease More News & Events What is Fabry Disease? Fabry disease is a rare, genetic condition which is estimated to affect
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Official Home Page of the Apellis Pharmaceuticals Corporate Site | Apellis Pharmaceuticals
Apellis is a global biopharmaceutical company that develops life-changing therapies. By pioneering targeted C3 therapies, we aim to treat diseases that are driven by excessive activation of the complement cascade, including those within hematology, ophthalmology, and nephrology.
Official Home Page of the Apellis Pharmaceuticals Corporate Site | Apellis Pharmaceuticals
Apellis is a global biopharmaceutical company that develops life-changing therapies. By pioneering targeted C3 therapies, we aim to treat diseases that are driven by excessive activation of the complement cascade, including those within hematology, ophthalmology, and nephrology.
MY HEALTH LEGACY
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Know Meningococcal
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Home | COVID-19 Information
Coronavirus disease 2019 (COVID-19) is a virus. Learn more about what this is and how it affects your community.
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Learn about Alnylam Pharmaceuticals, RNAi therapeutics, and the company's efforts in treating amyloidosis, hyperoxaluria, and porphyria.
Gout Patients
Have you been diagnosed with gout? Feel free to visit my blog and learn a thing about this disease.
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Coca Tea is Nature's gift to health and happiness. Learn more about how this obscure herb brings energy, healing, and even treats symptoms of serious diseases.
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Welcome to OnePath.com
Takeda's OnePath® is committed to providing personalized product support services to patients and their caregivers affected by rare diseases. Learn more about how we can help.
At-Home DNA Analysis and Genetic Testing | 3X4 Genetics
3x4 Genetics offers DNA genetic testing that tells you everything you need to know about your body. Learn how to manage your health with DNA testing.
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Atlanta's Complete Primary Care Physicians We specialize in the practice of adult medicine and the prevention and treatment of adult diseases. Before entering private practice, each of us dedicated at least three years of our medical training specifically learning how to prevent, diagnose, and treat diseases that
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Impacting the lives of children diagnosed with rare diseases by funding research and offering scholarships for alternative therapy. DONATE NOW in the news … Lucas was recently featured on Good Morning America! Visit Lucas’s page on GMA RESEARCH Research for Rare Disease There are approximately 7,000 known rare diseases in the United States, with an…
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