FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term intestinal hypomagnesemia 1 ID (Ontology) DOID:0060883 (Human Disease)
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.
Also Known As "HOMG1" ; "hypomagnesemia caused by selective magnesium malabsorption" ; "hypomagnesemia intestinal type 1" (for all, see Synonyms field below)
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 Genes
 intestinal hypomagnesemia 1       1
 for disease ribbon | intestinal hypomagnesemia 1       1
 model of | intestinal hypomagnesemia 1       1
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  metal metabolism disorder
   |__primary hypomagnesemia
       |__intestinal hypomagnesemia 1  1 rec.
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Synonyms
  • "HOMG1" EXACT OMO:0003012
    "hypomagnesemia caused by selective magnesium malabsorption" EXACT
    "hypomagnesemia intestinal type 1" EXACT
    "hypomagnesemic tetany" EXACT
    "intestinal hypomagnesemia with secondary hypocalcemia" EXACT
    "primary hypomagnesemia with secondary hypocalcemia" EXACT
Secondary IDs
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ICD10CM:E83.4
MIM:602014
ORDO:30924