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View history; General What links here; Related changes; ... This is a list of diseases starting with the letter "U". Ud–Up. UDP-galactose-4-epimerase deficiency ...
Widespread non-communicable diseases such as cardiovascular disease and cancer are not included. An epidemic is the rapid spread of disease to a large number of people in a given population within a short period of time; in meningococcal infections , an attack rate in excess of 15 cases per 100,000 people for two consecutive weeks is considered ...
Disease Discoverer 2600 BC: Malaria [1] 1900 BC: Rabies: 1600 BC: Cancer: Hippocrates: ca 300: Dengue: Jin Dynasty (266–420) 9th century: Measles: Muhammad ibn Zakariya al-Razi: 14th century: African trypanosomiasis: First described by Arab traders [2] 1798: Color blindness: John Dalton: 1798: Amyotrophic lateral sclerosis: John Dalton: 1881 ...
Hand, foot and mouth disease (HFMD) A diagnosis usually can be made by the presenting signs and symptoms alone. If the diagnosis is unclear, a throat swab or stool specimen may be taken. Medications are usually not needed as hand, foot, and mouth disease is a viral disease that typically resolves on its own. Under research [15] [16] Sin Nombre ...
GBS disease Group B Streptococcal disease: GCE Glycine encephalopathy: GD Gestational diabetes: GERD Gastroesophageal reflux disease: GI Gastrointestinal: GIB Gastrointestinal bleeding: GN Glossopharyngeal neuralgia: GORD Gastro-oesophageal reflux disease: GSS disease Gerstmann–Sträussler–Scheinker disease: GT/LD Gifted and learning ...
Airborne disease, a disease that spreads through the air. Contagious disease, a subset of infectious diseases. Cryptogenic disease, a disease whose cause is currently unknown. Disseminated disease, a disease that is spread throughout the body. Environmental disease; Lifestyle disease, a disease caused largely by lifestyle choices.
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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.