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DO Term : intestinal hypomagnesemia 1 [DOID:0060883] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

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.

synonyms:
HOMG1,
hypomagnesemic tetany,
ORDO:30924,
intestinal hypomagnesemia with secondary hypocalcemia,
hypomagnesemia intestinal type 1,
ICD10CM:E83.4,
hypomagnesemia caused by selective magnesium malabsorption,
602014,
primary hypomagnesemia with secondary hypocalcemia,
OMIM:602014

Disease

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Ontology

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