Search results
Results from the WOW.Com Content Network
This category reflects the organization of International Statistical Classification of Diseases and Related Health Problems, 10th Revision. Generally, diseases outlined within the ICD-10 codes R70-R79 within Chapter XVIII: Symptoms, signs and abnormal clinical and laboratory findings should be included in this category.
There are two types of Alpha-thalassemia, named hemoglobin Bart hydrops fetalis syndrome (also known as Hb Bart syndrome) and HbH disease. [22] Anemia: D50-D64: 663: Anemia is a type of medical condition that results in a decrease in the number of red blood cells (RBCs) or less than the normal quantity of hemoglobin in the blood. [2] Anemia of ...
The ICD-10-CM is generally the most widely used standard by insurance companies and hospitals who have to communicate with one another, for giving a overview of medical tests and procedures. It has over 70,000 codes. This list is not exhaustive but might be useful as a guide, even though it is not yet categorized consistently and only partly ...
ICD-10 is the 10th revision of the International Classification of Diseases (ICD), a medical classification list by the World Health Organization (WHO). It contains codes for diseases, signs and symptoms, abnormal findings, complaints, social circumstances, and external causes of injury or diseases. [1]
This is a shortened version of the fourth chapter of the ICD-9: Diseases of the Blood and Blood-forming Organs. It covers ICD codes 280 to 289. The full chapter can be found on pages 167 to 175 of Volume 1, which contains all (sub)categories of the ICD-9. Volume 2 is an alphabetical index of Volume 1.
As per guidelines of National AIDS Control Organisation (NACO) for accurate results & mass screening, [citation needed] analysis using hemoglobinometer is a recommended method used for absorbance measurement of whole blood at Hb/HbO2/Isobestic point, [citation needed] based on microcuvette technology such as HemoCue 301 [6] and Mokshit-Chanda ...
The recommended restrictive threshold for blood transfusion is a hemoglobin level of 7 to 8 g/dL, while a more liberal threshold is set at 9 to 10 g/dL. [10] However, more evidence may be required to establish a consensus on the threshold and a personalized approach may be more useful. [ 11 ]
People who have hemoglobin E/β-thalassemia have inherited one gene for hemoglobin E from one parent and one gene for β-thalassemia from the other parent. Hemoglobin E/β-thalassemia is a severe disease, and it still has no universal cure. However, the mutation is amenable to genome editing at high efficiency in preclinical studies. [6]