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(OMIM) | Defect in renal tubular reabsorption of Mg(2+) | 1 / 7739 | ||||
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(OMIM) | Low levels of serum Mg(2+) in the absence of other electrolyte disturbances | 1 / 7739 | ||||
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(HPO:0000006) | Autosomal dominant inheritance | 2518 / 7739 | ||||
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(HPO:0001324) | Muscle weakness | 859 / 7739 | ||||
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(HPO:0002315) | Headache | 175 / 7739 | ||||
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(HPO:0002321) | Vertigo | 58 / 7739 | ||||
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(HPO:0002917) | Hypomagnesemia | 19 / 7739 |