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Generally, diseases outlined within the ICD-10 codes E50-E56 within Chapter IV: Endocrine, nutritional and metabolic diseases should be included in this category. Subcategories This category has only the following subcategory.
Generally, diseases outlined within the ICD-10 codes E50-E64 within Chapter IV: Endocrine, nutritional and metabolic diseases should be included in this category. Wikimedia Commons has media related to Nutritional deficiencies .
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]
Holocarboxylase synthetase deficiency is an inherited metabolic disorder in which the body is unable to use the vitamin biotin effectively. [2] This disorder is classified as a multiple carboxylase deficiency , a group of disorders characterized by impaired activity of certain enzymes that depend on biotin.
Generally, diseases outlined within the ICD-10 codes E70-E72 within Chapter IV: Endocrine, nutritional and metabolic diseases should be included in this category. The main article for this category is Inborn errors of amino acid metabolism .
Common variable immunodeficiency (CVID) is an inborn immune disorder characterized by recurrent infections and low antibody levels, specifically in immunoglobulin (Ig) types IgG, IgM, and IgA. [2] Symptoms generally include high susceptibility to pathogens, chronic lung disease , as well as inflammation and infection of the gastrointestinal tract.
WHO ICD-11 release version – A searchable online version of ICD-11 that allows users to search by hierarchy or by entering the disease name. [6] WHO ICD-10 Version: 2019 – A searchable online version of ICD-10 that allows users to search by hierarchy or by entering the disease name. [7] List of Official ICD-10 Updates - ICD-10 updates ...
Familial isolated vitamin e deficiency; Other names: Ataxia With Vitamin E Deficiency: Familial isolated vitamin E deficiency has an autosomal recessive pattern of inheritance. Specialty: Neurology Treatment: high-dose oral vitamin E supplementation