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renal hypomagnesemia 6 (DOID:0060884)
Annotations: Rat: (1) Mouse: (1) Human: (1) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1)
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  
renal hypomagnesemia 3  
renal hypomagnesemia 4  
renal hypomagnesemia 5 with ocular involvement  
renal hypomagnesemia 6  
A hypomagnesemia characterized by autosomal dominant inheritance of severely lowered serum magnesium levels without other electrolyte disturbances or abnormalities in urinary magnesium excretion that has material_basis_in heterozygous mutation in the CNNM2 gene on chromosome 10q24. (DO)
Renal Hypouricemia  
Renal Hypouricemia, 2  
renal tubular acidosis +   
X-linked nephrolithiasis type I  

Exact Synonyms: HOMG6
Broad Synonyms: renal hypomagnesemia, dominant
Primary IDs: OMIM:613882
Xrefs: GARD:12155 ;   ICD10CM:E83.4
Definition Sources: "DO" "DO"

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