Term Name: renal hypomagnesemia 6
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 )

Relationships
is a type of: primary hypomagnesemia