Ad
related to: a list of rare diseases- HCP and Patient Resources
Helpful Resources. Education
and Support. cGVHD Patient Stories.
- cGVHD Manifestations
Impacts of Inflammation &
Fibrosis. Learn More Today.
- Clinical Study Data
Real-World Demographic of Patients.
See Results From a Pivotal Trial.
- MOA
Learn About This Treatment
Option's Mechanism of Action.
- HCP and Patient Resources
Search results
Results From The WOW.Com Content Network
A rare disease is technically defined (in the European Union) as a disease that is found in fewer than 5 people per every 10,000 people. ...
A rare disease is any 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 ...
Familial Alzheimer-like prion disease; Febrile infection-related epilepsy syndrome; Felty's syndrome; Fetal hydantoin syndrome; Fetal trimethadione syndrome; FG syndrome; Fitz-Hugh–Curtis syndrome; Fitzsimmons–Guilbert syndrome; Fleischer's syndrome; Floating–Harbor syndrome; Fountain syndrome; Franceschetti–Klein syndrome; Frank–Ter ...
The good news: there is more knowledge now about many of these rare diseases, and research into rare diseases is ongoing, through initiatives like the Rare Diseases Clinical Research Network ...
There are few times when your doctor or physician will utter the phrase, "I don't know" to a patient, but when you're dealing with the rarest of diseases, then all bets are off. According to the ...
This article provides a list of autoimmune diseases. These conditions, where the body's immune system mistakenly attacks its own cells, affect a range of organs and systems within the body. Each disorder is listed with the primary organ or body part that it affects and the associated autoantibodies that are typically found in people diagnosed ...
The following is a list of genetic disorders and if known, type of mutation and for the chromosome involved. Although the parlance "disease-causing gene" is common, it is the occurrence of an abnormality in the parents that causes the impairment to develop within the child. There are over 6,000 known genetic disorders in humans.
Any disease that impacts 200,000 people or less in the U.S. is classified as a rare disease. The rare disease community is a close-knit group of patients, parents and specialists determined to ...