Source: ALL
Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
CUI: C0268451
Disease: Manz syndrome
Manz syndrome 		2 0 2 0.33 0 0
CUI: C2673444
Disease: Hypocitraturia
Hypocitraturia 		2 2 2 0.33 1 0.50
CUI: C4510731
Disease: Familial primary hypomagnesemia with normocalciuria and normocalcemia
Familial primary hypomagnesemia with normocalciuria and normocalcemia 		2 0 2 0.33 0 0
CUI: C2673441
Disease: Renal calcium wasting
Renal calcium wasting 		3 0 2 0.29 0 0
CUI: C4552839
Disease: Hypomagnesemia, CTCAE
Hypomagnesemia, CTCAE 		21 0 6 0.29 0 0
CUI: C3715128
Disease: HYPOCALCEMIA, AUTOSOMAL DOMINANT 1
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1 		5 0 2 0.22 0 0
CUI: C3875492
Disease: Hypocalciuric hypercalcemia
Hypocalciuric hypercalcemia 		5 0 2 0.22 0 0
CUI: C4552089
Disease: HYPOCALCEMIA, AUTOSOMAL DOMINANT 1, WITH BARTTER SYNDROME
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1, WITH BARTTER SYNDROME 		5 0 2 0.22 0 0
CUI: C0271846
Disease: Familial hyperparathyroidism
Familial hyperparathyroidism 		7 0 2 0.18 0 0
CUI: C1522135
Disease: Hypermagnesemia result
Hypermagnesemia result 		7 0 2 0.18 0 0
CUI: C4554647
Disease: Hypermagnesemia, CTCAE
Hypermagnesemia, CTCAE 		7 0 2 0.18 0 0
CUI: C0012716
Disease: Disorder of magnesium metabolism
Disorder of magnesium metabolism 		1 0 1 0.17 0 0
CUI: C0037768
Disease: Spasmophilia
Spasmophilia 		1 0 1 0.17 0 0
CUI: C0086492
Disease: J-Pouch
J-Pouch 		1 0 1 0.17 0 0
CUI: C0270075
Disease: Perinatal disorder
Perinatal disorder 		1 0 1 0.17 0 0
CUI: C0270224
Disease: Tetany, Neonatal
Tetany, Neonatal 		1 0 1 0.17 0 0
CUI: C0332977
Disease: Congenital hemangiomatosis
Congenital hemangiomatosis 		1 0 1 0.17 0 0
CUI: C0595928
Disease: Serum calcium increased
Serum calcium increased 		1 0 1 0.17 0 0
CUI: C0917812
Disease: Tetanilla
Tetanilla 		1 0 1 0.17 0 0
CUI: C1820738
Disease: Feeding intolerance
Feeding intolerance 		1 0 1 0.17 0 0
CUI: C1832612
Disease: Hypocalcemia, Autosomal Dominant, with Bartter Syndrome
Hypocalcemia, Autosomal Dominant, with Bartter Syndrome 		1 0 1 0.17 0 0
CUI: C1832648
Disease: Hypoparathyroidism familial isolated
Hypoparathyroidism familial isolated 		8 0 2 0.17 0 0
CUI: C1840347
Disease: HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II (disorder)
HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE II (disorder) 		1 0 1 0.17 0 0
CUI: C1855466
Disease: Hypomagnesemia 5, Renal, with Ocular Involvement
Hypomagnesemia 5, Renal, with Ocular Involvement 		1 0 1 0.17 0 0
CUI: C2673648
Disease: Hypomagnesemia 4, Renal
Hypomagnesemia 4, Renal 		1 0 1 0.17 0 0