Websites using rare disorders as a keyword

Rare disease information gateway, support groups directory, practical advice, health and disability resources, research information, news and issues.

international, quarterly, peer reviewed journal that keeps cardiologists up to date with rare disorders of heart and vessels.

Dr. John G. McHenry is committed to the treatment, prevention and rehabilitation of neurologically related eye diseases and vision disorders. He is a leading Interventional Neuro-ophthalmologist who has trained the next generation of eye doctors in Oculoplastics, Orbital Surgery and the medical and surgical care of double vision. Dr. McHenry is the only interventional neuro-ophthalmologist in North Texas. He sees patient from all over North, East and West Texas as well as the Hill country, the Valley, the Panhandle, New Mexico, Oklahoma, Arkansas, Kansas, Missouri, Louisiana and Mississippi and consults on rare and complicated eye conditions across the country.

Join the National Organization for Rare Disorders (NORD) in raising awareness for the 30 million patients with rare diseases in the U.S. on Rare Disease Day®.

Chromosome Disorder Outreach, Inc. (CDO) is a non-profit organization for families affected by any type of rare chromosome disorder: deletions, translocations, trisomies, rings and inversions.

Charity helping parents of disabled children, including rare disorder, chronic syndrome, child behavioural problem or a chemical imbalance disability

Skin-diseases.org helps you to get complete cure for various skin diseases and disorders types, problems and common conditions including treatment methods and prevention tips.

Myasthenia Gravis Foundation of Michigan is committed to finding a cure for Myasthenia Gravis and closely related disorders, improving treatment options and providing information and support to people with Myasthenia Gravis through research, education, community programs, and advocacy.

Parent Project Muscular Dystrophy's mission is to end Duchenne muscular dystrophy. We accelerate research, raise our voices in Washington, demand optimal care for all young men, and educate the global community.

Providing video documentaries as well as articles and photographs to facilitate the diagnosis, treatment and education of individuals with rare or difficult to diagnose disorders.

NORD, a 501(c)(3) organization, is the leading patient advocacy organization dedicated to improving the lives of individuals and families living with rare diseases.

Lysosomal Diseases New Zealand

We are a Swiss specialty pharmaceutical company committed to developing medicines to meet the needs of patients living with mitochondrial disorders and other rare diseases.