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This is a shortened version of the third chapter of the ICD-9: Endocrine, Nutritional and Metabolic Diseases, and Immunity Disorders.It covers ICD codes 240 to 279.The full chapter can be found on pages 145 to 165 of Volume 1, which contains all (sub)categories of the ICD-9.
Monoisotopic mass is the sum of the masses of the atoms in a molecule using the most abundant isotope for each element; Monoisotopic element is one of the 26 chemical elements which have only one stable isotope
The monoisotopic mass is very useful when analyzing small organic compounds since compounds with similar weights will not be differentiated if the nominal mass is used. For example, when comparing tyrosine which has a molecular structure of C 9 H 11 NO 3 with a monoisotopic mass of 182.081 Da and methionine sulphone C 5 H 11 NO 4 S which ...
A fasting blood sugar level of ≥ 7.0 mmol / L (126 mg/dL) is used in the general diagnosis of diabetes. [17] There are no clear guidelines for the diagnosis of LADA, but the criteria often used are that the patient should develop the disease in adulthood, not need insulin treatment for the first 6 months after diagnosis and have autoantibodies in the blood.
IDDM11 (insulin-dependent diabetes mellitus 11) is one of the susceptibility genes for IDDM which locates on chromosome 14q24.3-q31. [ 2 ] [ 6 ] This loci is identified by linkage to D14S67 marker via a sibling-pair linkage analysis [ 2 ] [ 6 ] Based on the previous study, the biological behavior of IDDM11is different to HLA region genes so ...
Download QR code; Print/export ... Molar mass: 807.339 g·mol −1 ... Tripalmitin is a triglyceride derived from the fatty acid palmitic acid. References ...
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 .
MODY 3 or HNF1A-MODY is a form of maturity-onset diabetes of the young.It is caused by mutations of the HNF1-alpha gene, a homeobox gene on human chromosome 12.This is the most common type of MODY in populations with European ancestry, [1] accounting for about 70% of all cases in Europe.