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 0.22 0 0
CUI: C2673444
Disease: Hypocitraturia
Hypocitraturia 		2 2 2 0.22 2 1.00
CUI: C1845169
Disease: Renal phosphate wasting
Renal phosphate wasting 		8 0 3 0.21 0 0
CUI: C1853271
Disease: HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY
HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY 		3 0 2 0.20 0 0
CUI: C2673441
Disease: Renal calcium wasting
Renal calcium wasting 		3 0 2 0.20 0 0
CUI: C0342642
Disease: Autosomal dominant hypophosphatemic rickets
Autosomal dominant hypophosphatemic rickets 		11 0 3 0.18 0 0
CUI: C0342749
Disease: GLYCOGEN STORAGE DISEASE Ic
GLYCOGEN STORAGE DISEASE Ic 		5 0 2 0.17 0 0
CUI: C2673443
Disease: Hypermagnesiuria
Hypermagnesiuria 		6 1 2 0.15 1 0.50
CUI: C1833667
Disease: Elevated alkaline phosphatase of bone origin
Elevated alkaline phosphatase of bone origin 		7 0 2 0.14 0 0
CUI: C1838663
Disease: Enlargement of the wrists
Enlargement of the wrists 		8 0 2 0.13 0 0
CUI: C1835171
Disease: Hypomagnesemia 2, renal
Hypomagnesemia 2, renal 		10 0 2 0.12 0 0
CUI: C0012716
Disease: Disorder of magnesium metabolism
Disorder of magnesium metabolism 		1 0 1 0.11 0 0
CUI: C0155477
Disease: Tympanosclerosis involving other combination of structures
Tympanosclerosis involving other combination of structures 		1 0 1 0.11 0 0
CUI: C0268066
Disease: Hepatic hemosiderosis
Hepatic hemosiderosis 		1 0 1 0.11 0 0
CUI: C0270250
Disease: Meconium peritonitis
Meconium peritonitis 		1 0 1 0.11 0 0
CUI: C0271848
Disease: Hyperparathyroidism due to vitamin D deficiency
Hyperparathyroidism due to vitamin D deficiency 		1 0 1 0.11 0 0
CUI: C0342643
Disease: Autosomal recessive hypophosphatemic vitamin D refractory rickets
Autosomal recessive hypophosphatemic vitamin D refractory rickets 		11 0 2 0.11 0 0
CUI: C0346405
Disease: Ectopic parathyroid adenoma
Ectopic parathyroid adenoma 		1 0 1 0.11 0 0
CUI: C0346408
Disease: Parathyroid hormone-related peptide-secreting tumor
Parathyroid hormone-related peptide-secreting tumor 		1 0 1 0.11 0 0
CUI: C0393745
Disease: Chronic post-traumatic headache
Chronic post-traumatic headache 		1 0 1 0.11 0 0
CUI: C0456126
Disease: Neonatal rickets
Neonatal rickets 		1 0 1 0.11 0 0
CUI: C0475187
Disease: Brown tumor of hyperparathyroidism
Brown tumor of hyperparathyroidism 		1 0 1 0.11 0 0
CUI: C0858925
Disease: Deafness labyrinthine
Deafness labyrinthine 		1 0 1 0.11 0 0
CUI: C1274923
Disease: Cutaneous hyperalgesia
Cutaneous hyperalgesia 		1 0 1 0.11 0 0
CUI: C1737223
Disease: Secondary hypoparathyroidism
Secondary hypoparathyroidism 		1 0 1 0.11 0 0