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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.
This is an alphabetically sorted list of medical syndromes. 1p36 deletion syndrome; 1q21.1 deletion syndrome; 1q21.1 duplication syndrome; 13q deletion syndrome;
There are well over 6,000 known genetic disorders, [4] and new genetic disorders are constantly being described in medical literature. [5] More than 600 genetic disorders are treatable. [6] Around 1 in 50 people are affected by a known single-gene disorder, while around 1 in 263 are affected by a chromosomal disorder. [7]
List of congenital disorders. 1 language. ... List of ICD-9 codes 740–759: congenital anomalies; Rare disease This page was ...
Rare genetic syndromes (1 C, 176 P) T. People with tetra-amelia syndrome (5 P) Pages in category "Rare syndromes" The following 200 pages are in this category, out of ...
An eponymous disease is a disease, disorder, condition, or syndrome named after a person, usually the physician or other health care professional who first identified the disease; less commonly, a patient who had the disease; rarely, a literary character who exhibited signs of the disease or an actor or subject of an allusion, as characteristics associated with them were suggestive of symptoms ...
Rare genetic syndromes (1 C, 171 P) Pages in category "Genetic syndromes" The following 164 pages are in this category, out of 164 total.
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 ...
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