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What Is the NORD Rare Disease Database? With more than 1,200 rare disorders, you can explore rare disease reports that include information on symptoms, causes, treatments, clinical trials, and sources of help such as patient advocacy organizations.
- Achalasia
Achalasia is a rare disorder that typically affects adults...
- Aarskog Syndrome
Noonan syndrome with multiple lentigines (NSML) is a rare...
- Acoustic Neuroma
Learn about Acoustic Neuroma, including symptoms, causes,...
- Abetalipoproteinemia
Abetalipoproteinemia is a rare inherited disorder affecting...
- Achondrogenesis
Disease Overview. Summary. Achondrogenesis is a group of...
- Aceruloplasminemia
Aceruloplasminemia is a rare genetic disorder characterized...
- Acanthocheilonemiasis
Acanthocheilonemiasis is a rare tropical infectious disease...
- Ablepharon-Macrostomia Syndrome
AMS has been grouped within the category of diseases called...
- Achalasia
Ohio - National Organization for Rare Disorders. Interested in giving the rare disease community in your state a voice in state government? Learn more about NORD’s work on Rare Disease Advisory Councils (RDACs) and how you can get involved with RDAC activities in your state. Summary.
Feb 1, 2023 · The Ohio Rare Disease Advisory Council (ORDAC) is established by section 103.60 of the Ohio Revised Code. The ORDAC consists of 31 members appointed by the Governor, the Speaker of the Ohio House of Representatives, and the President of the Ohio Senate.
Learn how a disease is defined as rare, why rare disease research is important, what causes rare diseases, and how you can help.
A rare disease is a disease that affects a small percentage of the population. In some parts of the world, the term orphan disease describes a rare disease whose rarity results in little or no funding or research for treatments, without financial incentives from governments or other agencies. Orphan drugs are medications targeting orphan diseases.
A rare disease is a disease that affects a small percentage of the population but there is no single accepted definition. The European Union and United Kingdom define a disease as rare if it affects fewer than 1 in 2,000 people, but there is no universal definition.
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Dec 3, 2019 · Nomi: There’s no single definition of “rare disease” because it depends on which region or group you’re talking about. In the U.S., a rare disease is legally defined as one that affects fewer than 200,000 people; in the EU, a rare disease is one that affects fewer than 1 in 2,000 people.