Term Name: | renal hypomagnesemia 6 |
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Synonyms: | HOMG6 |
Definition: | A hypomagnesemia characterized by autosomal dominant inheritance of severely lowered serum magnesium levels without other electrolyte disturbances or abnormalities in urinary magnesium excretion that has_material_basis_in heterozygous mutation in the CNNM2 gene on chromosome 10q24. |
Ontology: | Human Disease [DOID:0060884] ( DOID:0060884 ) |