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  2. Category:Vitamin deficiencies - Wikipedia

    en.wikipedia.org/wiki/Category:Vitamin_deficiencies

    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.

  3. Category:Nutritional deficiencies - Wikipedia

    en.wikipedia.org/wiki/Category:Nutritional...

    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 .

  4. Category:Amino acid metabolism disorders - Wikipedia

    en.wikipedia.org/wiki/Category:Amino_acid...

    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 .

  5. ICD-10 - Wikipedia

    en.wikipedia.org/wiki/ICD-10

    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]

  6. Holocarboxylase synthetase deficiency - Wikipedia

    en.wikipedia.org/wiki/Holocarboxylase_synthetase...

    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.

  7. Beta-ketothiolase deficiency - Wikipedia

    en.wikipedia.org/wiki/Beta-ketothiolase_deficiency

    Beta-ketothiolase deficiency is a rare, autosomal recessive metabolic disorder in which the body cannot properly process the amino acid isoleucine or the products of lipid breakdown. [ 1 ] [ 2 ] Along with SCOT deficiency , it belongs to a group of disorders called ketone utilisation disorders.

  8. ICD coding for rare diseases - Wikipedia

    en.wikipedia.org/wiki/ICD_coding_for_rare_diseases

    Europe and other parts of the world use the ICD-10. The root codes for ICD-10 and ICD-10-CM are the same, making it helpful for locating codes for general body systems and disease processes. [2] [3] In ICD-11 the search and coding of any disease, including rare ones is done via the ICD-11 website. [4]

  9. Histidinemia - Wikipedia

    en.wikipedia.org/wiki/Histidinemia

    Histidinemia is a rare autosomal recessive metabolic disorder caused by a deficiency of the enzyme histidase. Histidase is needed for the metabolism of the amino acid histidine . [ 1 ] Although originally thought to be linked to multiple developmental disorders histidinemia is now accepted as a relatively benign disorder, [ 2 ] leading to a ...