Ads
related to: extremely rare genetic diseases list
Search results
Results from the WOW.Com Content Network
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.
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 ...
Pages in category "Rare genetic syndromes" The following 176 pages are in this category, out of 176 total. ... Autosomal dominant leukodystrophy with autonomic disease;
An example is cystic fibrosis, a genetic disease: it is rare in most parts of Asia but relatively common in Europe and in populations of European descent. In smaller communities, the founder effect can result in a disease that is very rare worldwide being prevalent within the smaller community. Many infectious diseases are prevalent in a given ...
It should directly contain very few, if any, pages and should mainly contain subcategories. The main article for this category is rare disease . 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.
They come in all shapes and sizes. Some walk, some slither, some fly and some swim. Humans are blessed to share the planet with just over 2.1 million recognized species of animals. And scientists ...
Ads
related to: extremely rare genetic diseases list