You are using an outdated browser. Please upgrade your browser to improve your experience.

autosomal recessive proximal renal tubular acidosis

Disease Summary
Associated Targets (1)


Mondo Description Autosomal recessive proximal renal tubular acidosis (AR pRTA) is a rare form of proximal renal tubular acidosis (pRTA) characterized by an isolated defect in the proximal tubule leading to the decreased reabsorption of bicarbonate and consequentially to urinary bicarbonate wastage along with additional characteristic clinical features.
Uniprot Description An extremely rare autosomal recessive syndrome characterized by short stature, profound proximal renal tubular acidosis, mental retardation, bilateral glaucoma, cataracts and bandkeratopathy. pRTA is due to a failure of the proximal tubular cells to reabsorb filtered bicarbonate from the urine, leading to urinary bicarbonate wasting and subsequent acidemia.
Mondo Term and Equivalent IDs
MONDO:0011422:  autosomal recessive proximal renal tubular acidosis