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Ontology Browser

Term:
Parent Terms Term With Siblings Child Terms
Bartter disease +   
Dent disease +   
Donnai-Barrow syndrome  
Familial Azotemia 
Familial Hypophosphatemia +   
Familial Renal Hypouricemia due to Tubular Hypersecretion  
Fanconi syndrome +   
Gitelman syndrome  
Hypomagnesemia, Hypertension, and Hypercholesterolemia, Mitochondrial  
Hypomagnesemia, Seizures, and Mental Retardation +   
hypophosphatemic nephrolithiasis/osteoporosis 2  
Hypouricemia, Hypercalcinuria, and Decreased Bone Density 
Iminoglycinuria  
Liddle syndrome +   
nephrogenic syndrome of inappropriate antidiuresis  
oculocerebrorenal syndrome +   
pseudohypoaldosteronism +   
Renal Aminoacidurias +   
A group of inherited kidney disorders characterized by the abnormally elevated levels of AMINO ACIDS in URINE. Genetic mutations of transport proteins result in the defective reabsorption of free amino acids at the PROXIMAL RENAL TUBULES. Renal aminoaciduria are classified by the specific amino acid or acids involved.
renal glycosuria +   
renal hypomagnesemia 2  
renal hypomagnesemia 4  
renal hypomagnesemia 5 with ocular involvement  
renal hypomagnesemia 6  
Renal Hypouricemia  
Renal Hypouricemia, 2  
renal tubular acidosis +   
X-linked nephrolithiasis type I  

Synonyms
Exact Synonyms: AMINOACIDURIA ;   Renal Aminoaciduria
Primary IDs: MESH:D000608 ;   RDO:0001224
Definition Sources: MESH:D000608

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