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Ontology Browser

Term:
intestinal hypomagnesemia 1 (DOID:0060883)
Annotations: Rat: (2) Mouse: (2) Human: (2) Chinchilla: (2) Bonobo: (2) Dog: (2) Squirrel: (2) Pig: (2)
Parent Terms Term With Siblings Child Terms
Hypocalcemia +     
autosomal dominant hypocalcemia +   
intestinal hypomagnesemia 1  
A hypomagnesemia characterized by very low serum magnesium levels due to defects in intestinal absorbtion and kidney excretion and secondary hypocalcemia that has material_basis_in homozygous or compound heterozygous mutations in the TRPM6 gene on chromosome 9q21. (DO)
Manz Syndrome 
renal hypomagnesemia 2  
renal hypomagnesemia 3  
renal hypomagnesemia 4  
renal hypomagnesemia 5 with ocular involvement  
renal hypomagnesemia 6  
Tetany  

Synonyms
Exact Synonyms: HOMG1 ;   HSH ;   HYPOMAGNESEMIC TETANY ;   Hypomagnesemia with Secondary Hypocalcemia ;   hypomagnesemia caused by selective magnesium malabsorption ;   hypomagnesemia intestinal type 1 ;   intestinal hypomagnesemia with secondary hypocalcemia ;   primary hypomagnesemia with secondary hypocalcemia
Primary IDs: MESH:C566593
Alternate IDs: OMIM:602014
Xrefs: ORDO:30924
Definition Sources: https://www.ncbi.nlm.nih.gov/pubmed/12032568 "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/12032570 "DO" "DO", https://www.ncbi.nlm.nih.gov/pubmed/18818955 "DO" "DO"

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