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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.
Download as PDF; Printable version; ... out of 187 total. This list may not reflect recent changes. ... List of genetic disorders; List of OMIM disorder codes; 0–9.
Pages for logged out editors learn more. Contributions; ... Download as PDF; Printable version; In other projects ... Autosomal recessive disorders (5 C, 441 P) M ...
List of human disease case fatality rates; List of notifiable diseases - diseases that should be reported to public health services, e.g., hospitals. Lists of plant diseases; List of pollution-related diseases; List of skin conditions; List of diseases by year of discovery; Disorders. List of communication disorders; List of genetic disorders ...
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 ...
Download as PDF; Printable version; In other projects ... This is a list of diseases starting with the letter "S ". Sa. Saa–Sal; Sam–Say; Saa–Sal ... genetic types;
Sickle cell disease is a group of inherited blood disorders, caused by a genetic abnormality in the oxygen-carrying protein haemoglobin found in red blood cells. [57] Under certain circumstances, this leads to the red blood cells adopting an abnormal sickle -like shape; with this shape, they are unable to deform as they pass through capillaries ...
The mode of inheritance of a particular disease is also recorded.. Each disease is represented with gene name, chromosome location, mutations, and geospatial distribution. The first version of the database covered 52 diseases with information on 5,760 individuals. [1] It later expanded to 109 genetic diseases.