| HYPOMAGNESEMIA 6, RENAL; HOMG6 | |
|
613882
OMIM = Online Mendelian Inheritance of Men | |
|
34527 | |
| Metal transporter CNNM2 | |
| rare autosomal dominant mutation in the CNNM2 gene | |
| Laboratory findings | Magnesium dec (serum) |
| Symptoms | headache (severe, recurrent or occipital, migraine) muscle weakness no clinical symptoms (probably) onset, adolescent onset, childhood onset, infancy vertigo, dizziness |