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The first version was developed in the early 1980s by Dr James Read, a Loughborough general medical practitioner. [2] The scheme was structured similarly to ICD-9: . each code was composed of four consecutive characters: first character 0-9, A-Z (excepting I and O), remaining three characters 0-9, A-Z/a-z (excepting i,I,o and O) plus up to three trailing period '.' characters
Hereditary angioedema (HAE) is a disorder that results in recurrent attacks of severe swelling. [3] The swelling most commonly affects the arms, legs, face, intestinal tract, and airway. [3] If the intestinal tract is affected, abdominal pain and vomiting may occur. [1] Swelling of the airway can result in its obstruction and trouble breathing. [1]
E831.1 Accident to watercraft causing other injury to occupant of small boat, powered; E831.2 Accident to watercraft causing other injury to occupant of other watercraft—crew; E831.3 Accident to watercraft causing other injury to occupant of other watercraft—other than crew; E831.4 Accident to watercraft causing other injury to water skier
Antiphospholipid syndrome is known for causing arterial or venous blood clots, in any organ system, and pregnancy-related complications.While blood clots and pregnancy complications are the most common and diagnostic symptoms associated with APS, other organs and body parts may be affected like platelet levels, heart, kidneys, brain, and skin.
Cardiogenic pulmonary edema is the result of cardiovascular insufficiency. Treatment is directed at improving cardiovascular function and providing supportive care. [ 43 ] [ 44 ] Positioning upright may relieve symptoms.
Hemoglobinopathy is the medical term for a group of inherited blood disorders involving the hemoglobin, the protein of red blood cells. [1] They are generally single-gene disorders and, in most cases, they are inherited as autosomal recessive traits. [2] [3]
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Hemoglobin H disease is a genetic disorder resulting in absent or impaired production of the α-globin protein, a normal component of the hemoglobin. The disease occurs when the α-globin gene expression is reduced to less than 30% of the normal expression. [2]