Search results
Results from the WOW.Com Content Network
This template allows editors to directly link to the 2019 online version of the World Health Organization's diagnostic classification ICD-10. It's primarily intended for use with {{medical resources}}. Please do not use this template to parse codes only found within ICD-10-CM – use the {} template instead.
Their red blood cells contain both hemoglobin C and either normal hemoglobin A or hemoglobin S. Hemoglobin C mutation is an autosomal recessive disorder that results from the biparental inheritance of the allele that encodes for hemoglobin C. [6] If both parents are carriers of hemoglobin C, there is a chance of having a child with hemoglobin C ...
This template is intended for use within {{Medical resources}}, and enables ICD-10-CM codes to be listed when they differ, or offer more specificity, from those in the international version. To list codes from the international version of ICD-10, and link to the World Health Organization website, please use {{ Template:ICD10 }}.
Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more
ICD-10 coding number Diseases Database coding number Medical Subject Headings Disseminated intravascular coagulation (DIC, defibrination syndrome) Protein C deficiency: Protein C deficiency is a rare genetic trait that predisposes to thrombotic disease. [83] Protein S deficiency: Factor V Leiden: Thrombocytosis: Idiopathic thrombocytopenic ...
Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more
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]
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.