Diseases

Renal Tubular Acidosis, Distal, Autosomal Dominant

renal tubular acidosis, distal, autosomal dominant

Basic Information

Grouped by core information, identifiers, and descriptions.

Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.

Description: NCI2016_NICHD_1602D:Impairment in renal collecting tubule acid secretion that results in a hypokalemic hyperchloremic metabolic acidosis.|NCI2016_NICHD_1602D:Failure of the renal tubules of the kidney to excrete urine of sufficient acidity, resulting in metabolic acidosis.|NCI2016_02D:Impairment in renal collecting tubule acid secretion that results in a hypokalemic hyperchloremic metabolic acidosis.(NICHD)|NCI2016_02D:Failure of the renal tubules of the kidney to excrete urine of sufficient acidity, resulting in metabolic acidosis.(NICHD)|MSH2017_2016_08_12:The genetic defect is in the anion exchange protein gene SLC4A1 resulting in impaired excretion of hydrogen ions or renal acids in the distal renal tubules.|HPO2016_07_04:A type of renal tubular acidosis characterized by a failure of acid secretion by the alpha intercalated cells of the cortical collecting duct of the distal nephron. The urine cannot be acidified below a pH of 5.3, associated with acidemia and hypokalemia. [HPO:probinson]

Direct relations and traceable candidates grouped by relation type.