136 Alternatives to globalgenes.org
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everylifefoundation.org
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sumairafoundation.org
Neuromyelitis Optica Spectrum Disorder (NMOSD) is a rare syndrome that affects the central nervous system as well as the spinal cord.
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NORD is dedicated to supporting education, elevating care, advancing research, and driving policy for rare diseases
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omim.org
Online Mendelian Inheritance in Man (OMIM) is a comprehensive, authoritative compendium of human genes and genetic phenotypes that is freely available and updated daily. The full-text, referenced overviews in OMIM contain information on all known mendelian disorders and over 15,000 genes. OMIM focuses on the relationship between phenotype and genotype. It is updated daily, and the entries contain copious links to other genetics resources.
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biomarin.com
Researches and develops therapies for debilitating, fatal, chronic genetic disorders causing enzyme deficiency of carbohydrate metabolism, such as phenylketonuria. Headquarters in Novato, California. (Nasdaq: BMRN).
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Weill Cornell Brain and Spine Center |
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The Merck Manuals (known as the MSD Manuals outside US & Canada) are the global standard in medical reference for Doctors, Students & Consumers - since 1899.
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debra.org.uk
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CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases.
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This is the homepage for Great Ormond Street Hospital Trust website.
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dermnetnz.org
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As the preeminent professional organization for digestive disorders, ACG is focused on advancing gastroenterology and improving patient care.
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Evidence-based clinical solutions from UpToDate are trusted by clinicians, professionals, and healthcare enterprises worldwide to enable the best possible care decisions and improve health outcomes.
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American Academy of Family Physicians represents 129,600 family physicians, residents, & students, providing advocacy, education, patient & practice resources.
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Pediatric teaching hospital of Harvard Medical School. Includes details of departments, clinics, and research, as well as information for patients and families. [Massachusetts]
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medlineplus.gov
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genome.gov
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Non-profit patient advocacy organization. Support and information provided for those affected by rare chromosome disorder.
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halyardhealth.com.au
Halyard, part of the Owens & Minor Global Products Division, is focused on moving care forward. Our $1.2 billion portfolio of market-leading brands includes HALYARD, MEDICHOICE, MEDICAL ACTION and AVID are sold in more than 90 countries. Halyard's broad portfolio offers the right product for each need, backed by best-in-class clinical expertise and more support at points of care. Our product standardization opportunities combined with supply chain expertise help drive efficiencies and protect healthcare providers from risks and disruptions in care.
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thinkgenetic.com
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bmj.com
High impact medical journal. Champion of better research, clinical practice & healthcare policy since 1840. For GPs, hospital doctors, educators, policymakers.
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Named a best children's hospital by U.S. News & World Report, CHOC is defining the future of pediatric medicine.
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parentprojectmd.org
Parent Project Muscular Dystrophy (PPMD) fights to end Duchenne muscular dystrophy. We accelerate research, raise our voices to impact policy, demand optimal care for every single family, and strive to ensure access to approved therapies.
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rareconnect.org
A safe, easy to use platform where rare disease patients, families and patient organizations can develop online communities and conversations across continents and languages. RareConnect partners with the world's leading rare disease patient groups to offer global online communities allowing people to connect around issues which affect them while living with a rare disease.
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centerwatch.com
The global source of news, directories, proprietary market research, and analysis for clinical trials professionals and patients.
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asap.org
Aims to improve the lives of persons affected by syringomyelia, Chiari malformation and related disorders.
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cureduchenne.org
Founded by parents of a patient, to raise funds for research. California.
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MDA is the #1 health nonprofit advancing research, care and advocacy for people living with muscular dystrophy, ALS, and related neuromuscular diseases.
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sarepta.com
We are focused on the development of precision genetic medicines to treat rare neuromuscular and central nervous system diseases. Learn more about Sarepta.
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ionispharma.com
Leading company in RNA-targeted drug discovery and development for rare/orphan diseases.
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managedhealthcareconnect.com
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pharmatimes.com
PharmaTimes was the first independent monthly magazine for the pharmaceutical, biotechnology and healthcare industries. Today, we are still the only UK publication that’s designed for and reaches all levels of Industry management – across all departments. And, to complement the magazine, we have launched our unique online PharmaTimes digital channel ( www.pharmatimes.com ), providing daily up-to-the-minute Industry news in video and text format, competition news and thousands of jobs online.
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Up to date news for the pharmaceutical and biotechnology industries - The Pharma Letter
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The Medical Letter has provided trusted prescription drug information and drug facts since 1959
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Provides health and medical services, ongoing research, and professional educational opportunities. [Ohio]
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fapnewstoday.com
FAP News Today Home - FAP News Today
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apfed.org
Group sharing information and resources about eosinophilic esophagitis, eosinophilic gastritis, hypereosinophilic syndrome, Churg Strauss syndrome, and chronic eosinophilic leukemia.
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amyloidosis.org
Provide complete, integrated, easy-to-reach support and information to existing information and referrals for other sources of help. Primarily for patients and their families struggling with the disease.
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ulf.org
Nonprofit, voluntary health organization dedicated to providing patients and their families with information about their disease and assistance in their health.
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vimizim.com
VIMIZIM® (elosulfase alfa) is the first and only enzyme replacement therapy approved for people with Morquio A. View important safety information, including risk of anaphylaxis.
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Mal de Débarquement, Disembarkment or Debarkation Syndrome is a disorder that leaves patients with a constant feeling of movement, as if on a boat. The MdDS Foundation advocates for and seeks treatments to end the suffering from MdDS. Learn more!
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genecards.org
A searchable, integrated database of human genes that provides concise genomic, proteomic, transcriptomic, genetic and functional information on all known and predicted human genes.
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umdf.org
To promote research for the cure and treatment, and to provide support to families. The UMDF offers a library, patient registry, support information, conferences, research and grant updates, and a special section for physicians.
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beyondachondroplasia.org
Achondroplasia is a rare bone condition that originates systemic effects that go beyond a growth problem. Beyond Achondroplasia shares the bridges that clarifies what happens inside the body and outside it, in the family and society.
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Biotech, drug, pharma and health news for business and professional readers
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UniProt
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American Academy of Dermatology
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proteinatlas.org
The Human Protein Atlas
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genenames.org
Home | HUGO Gene Nomenclature Committee
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mayoclinic.org
Top-ranked Hospital in the Nation - Mayo Clinic
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aocd.org
Information on this organization, health of the skin, and finding an osteopathic dematologist.
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skinsight.com
Skincare, skin health, and skin disease insights from experts
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mastcellaction.org
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patient.info
The same info as provided by GPs to patients during consultations,health/disease leaflets,patient support orgs,all about medicines,book GP appts online,interactive patient experience forum
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misophonia.com
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rare-diseases.eu
The ECRD is recognised globally as the largest, patient-led rare disease policy event in which collaborative dialogue, learning and conversation takes place, forming the groundwork to shape goal-driven rare disease policies and allow for important and innovative discussions on a national and an international level to take place.
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misophoniainstitute.org
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Neurology Times
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jamanetwork.com
Stay up to date, maintain your CME with the latest research, author interviews, apps, and learning courses from JAMA and the Specialty Journals.