Search Ontology:
Human Disease

intestinal hypomagnesemia 1

Term ID
DOID:0060883
Synonyms
  • HOMG1
  • hypomagnesemia caused by selective magnesium malabsorption
  • hypomagnesemia intestinal type 1
  • hypomagnesemic tetany
  • intestinal hypomagnesemia with secondary hypocalcemia
  • primary hypomagnesemia with secondary hypocalcemia
Definition
A hypomagnesemia characterized by very low serum magnesium levels due to defects in intestinal absorption and kidney excretion and secondary hypocalcemia that has_material_basis_in homozygous or compound heterozygous mutations in the TRPM6 gene on chromosome 9q21. (3)
References
Ontology
Human Disease   ( DOID:0060883 )
Relationships
is a type of
Other Pages
Alliance (1)
Genes Involved
Zebrafish Models
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