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renal hypomagnesemia 2 (DOID:0060885)
Annotations: Rat: (2) Mouse: (2) Human: (3) Chinchilla: (2) Bonobo: (1) Dog: (2) Squirrel: (2) Pig: (2)
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  
hypophosphatemic nephrolithiasis/osteoporosis 2  
Hypouricemia, Hypercalcinuria, and Decreased Bone Density 
intestinal hypomagnesemia 1  
Liddle syndrome +   
Manz Syndrome 
nephrogenic syndrome of inappropriate antidiuresis  
oculocerebrorenal syndrome +   
pseudohypoaldosteronism +   
Renal Aminoacidurias +   
renal glycosuria +   
renal hypomagnesemia 2  
A hypomagnesemia characterized by autosomal dominant inheritance of hypomagnesemia due to renal magnesium loss that has material_basis_in heterozygous mutation in the FXYD2 gene on chromosome 11q23. (DO)
renal hypomagnesemia 3  
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  

Exact Synonyms: HOMG2 ;   autosomal dominant primary hypomagnesemia with hypocalciuria ;   magnesium loss, isolated renal ;   magnesium wasting, renal
Broad Synonyms: renal hypomagnesemia, dominant
Primary IDs: MESH:C537152
Alternate IDs: OMIM:154020
Xrefs: GARD:3350 ;   ORDO:34528
Definition Sources: "DO" "DO", "DO" "DO"

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