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Ontology Browser

Term:
hypophosphatemic nephrolithiasis/osteoporosis 2 (DOID:0080078)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
Parent Terms Term With Siblings Child Terms
Azotemia, Familial 
Bartter disease +   
Dent disease +   
Donnai-Barrow syndrome  
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 1  
hypophosphatemic nephrolithiasis/osteoporosis 2  
Hypouricemia, Hypercalcinuria, and Decreased Bone Density 
Iminoglycinuria  
Liddle syndrome +   
oculocerebrorenal syndrome +   
pseudohypoaldosteronism +   
Renal Aminoacidurias +   
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 +   

Synonyms
Exact Synonyms: NPHLOP2
Primary IDs: MESH:C567362
Alternate IDs: OMIM:612287 ;   RDO:0009619 ;   RDO:0015453

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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.