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intestinal hypomagnesemia 1 (DOID:0060883)
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Synonyms: HOMG1; hypomagnesemia caused by selective magnesium malabsorption; hypomagnesemia intestinal type 1; hypomagnesemic tetany; intestinal hypomagnesemia with secondary hypocalcemia; primary hypomagnesemia with secondary hypocalcemia
Alt IDs: OMIM:602014, ICD10CM:E83.4, ORDO:30924
Definition: 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.

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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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