isolated autosomal dominant hypomagnesemia, Glaudemans type ICD10:E83.4 Isolated autosomal dominant hypomagnesemia, Glaudemans type (IADHG) is a form of familial primary hypomagnesemia (FPH), characterized by low serum magnesium (Mg) values but normal urinary Mg values. The typical clinical features are recurrent muscle cramps, episodes of tetany, tremor, and muscle weakness, especially in distal limbs. The disease is potentially fatal. MONDO:0016048 Orphanet:199326 SCTID:722008003 UMLS:CN200728 familial primary hypomagnesemia with normocalcuria