Inborn errors of renal tubular transport are metabolic disorders which lead to impairment in the ability of solutes, such as salts or amino acids, to... 1 KB (57 words) - 15:55, 8 July 2021 |
 | into the lumen of renal tubule. Tubular secretion can be either active or passive or co-transport. Substances mainly secreted into renal tubule are; H+... 22 KB (1,917 words) - 17:07, 31 December 2023 |
 | Kidney stone disease (redirect from Renal calculus) (June 1968). "Familial iminoglycinuria. An inborn error of renal tubular transport". The New England Journal of Medicine. 278 (26): 1407–13. doi:10... 132 KB (13,804 words) - 20:06, 28 April 2024 |
 | Iminoglycinuria is an autosomal recessive disorder of renal tubular transport affecting reabsorption of the amino acid glycine, and the imino acids proline... 22 KB (2,573 words) - 20:24, 31 December 2023 |
Homeostasis (redirect from Wisdom of the Body) reabsorption of sodium ions from the tubular fluid as a result of high aldosterone levels in the blood does not, of itself, cause renal tubular water to be... 80 KB (9,670 words) - 12:52, 29 April 2024 |
 | Systemic primary carnitine deficiency (SPCD) is an inborn error of fatty acid transport caused by a defect in the transporter responsible for moving carnitine... 12 KB (1,279 words) - 09:22, 11 April 2023 |
 | Glycogen storage disease (category Inborn errors of carbohydrate metabolism) of cause: genetic and environmental. Genetic GSD is caused by any inborn error of carbohydrate metabolism (genetically defective enzymes or transport... 65 KB (5,883 words) - 18:49, 21 April 2024 |
 | Glycogen storage disease type I (redirect from Hepato-renal glycogenesis) multiple derangements of renal tubular reabsorption, including tubular acidosis with bicarbonate and phosphate wasting. These tubular abnormalities in GSD... 45 KB (5,801 words) - 07:01, 15 April 2024 |
419.795 – renal osteodystrophy MeSH C12.777.419.815 – renal tubular transport, inborn errors MeSH C12.777.419.815.093 – acidosis, renal tubular MeSH C12... 18 KB (1,422 words) - 16:48, 9 February 2024 |
851 – renal tubular transport, inborn errors MeSH C18.452.648.851.093 – acidosis, renal tubular MeSH C18.452.648.851.191 – aminoaciduria, renal MeSH C18... 47 KB (4,274 words) - 16:49, 9 February 2024 |
851 – renal tubular transport, inborn errors MeSH C16.320.565.851.093 – acidosis, renal tubular MeSH C16.320.565.851.191 – aminoaciduria, renal MeSH C16... 78 KB (6,496 words) - 05:23, 12 April 2022 |
 | Lysine (category CS1 errors: missing periodical) of renal tubular transport. Lysine production for animal feed is a major global industry, reaching in 2009 almost 700,000 tons for a market value of over... 68 KB (7,502 words) - 20:02, 4 May 2024 |
 | Glycogen storage disease type V (category Inborn errors of carbohydrate metabolism) disease Hitting the wall (muscle fatigue due to glycogen depletion) Inborn errors of carbohydrate metabolism Purine nucleotide cycle§Glycogenoses (GSDs)... 58 KB (6,597 words) - 05:23, 13 May 2024 |