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| Term | renal hypomagnesemia 2 | ID (Ontology) | DOID:0060885 (Human Disease) |
| Definition | A hypomagnesemia characterized by autosomal dominant inheritance of hypomagnesemia due to renal magnesium loss that has_material_basis_in heterozygous mutation in the FXYD2 gene on chromosome 11q23. | ||
| Also Known As | "autosomal dominant primary hypomagnesemia with hypocalciuria" ; "HOMG2" | ||
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metal metabolism disorder |__primary hypomagnesemia |__renal hypomagnesemia 2 |
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| Is a | primary hypomagnesemia | ||
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GARD:3350 ICD10CM:E83.4 MIM:154020 ORDO:34528 |
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