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: C0853241
Disease: Exacerbation of anxiety
Exacerbation of anxiety 		1 0 1 0.33 0 0
CUI: C1855801
Disease: Calcium nephrolithiasis
Calcium nephrolithiasis 		1 0 1 0.33 0 0
CUI: C2676786
Disease: Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1
Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1 		1 0 1 0.33 0 0
CUI: C3150652
Disease: FANCONI RENOTUBULAR SYNDROME 2
FANCONI RENOTUBULAR SYNDROME 2 		1 0 1 0.33 0 0
CUI: C0268709
Disease: Renal tubular defect
Renal tubular defect 		2 0 1 0.25 0 0
CUI: C0342635
Disease: Hungry bone syndrome
Hungry bone syndrome 		2 0 1 0.25 0 0
CUI: C4310232
Disease: Hypercalcemia, Infantile, 1
Hypercalcemia, Infantile, 1 		2 0 1 0.25 0 0
CUI: C4310473
Disease: Hypercalcemia, infantile, 2
Hypercalcemia, infantile, 2 		2 0 1 0.25 0 0
CUI: C4551503
Disease: FANCONI RENOTUBULAR SYNDROME 1
FANCONI RENOTUBULAR SYNDROME 1 		2 0 1 0.25 0 0
CUI: C1845169
Disease: Renal phosphate wasting
Renal phosphate wasting 		8 0 2 0.22 0 0
CUI: C0268080
Disease: Hypercalcemia, Idiopathic, of Infancy
Hypercalcemia, Idiopathic, of Infancy 		3 0 1 0.20 0 0
CUI: C0348454
Disease: Other hypoparathyroidism
Other hypoparathyroidism 		3 0 1 0.20 0 0
CUI: C0403477
Disease: Medullary nephrocalcinosis
Medullary nephrocalcinosis 		9 0 2 0.20 0 0
CUI: C1265884
Disease: Eggshell calcium deposition
Eggshell calcium deposition 		3 0 1 0.20 0 0
CUI: C1833331
Disease: Increased serum 1,25-dihydroxyvitamin D3
Increased serum 1,25-dihydroxyvitamin D3 		3 0 1 0.20 0 0
CUI: C0265374
Disease: Warfarin syndrome
Warfarin syndrome 		4 0 1 0.17 0 0
CUI: C1838659
Disease: Deformed rib cage
Deformed rib cage 		4 0 1 0.17 0 0
CUI: C1848538
Disease: Bulging of the costochondral junction
Bulging of the costochondral junction 		4 0 1 0.17 0 0
CUI: C2874202
Disease: Constitutional delay of puberty
Constitutional delay of puberty 		4 0 1 0.17 0 0
CUI: C3888204
Disease: ACTN3 DEFICIENCY
ACTN3 DEFICIENCY 		4 0 1 0.17 0 0
CUI: C0342749
Disease: GLYCOGEN STORAGE DISEASE Ic
GLYCOGEN STORAGE DISEASE Ic 		5 0 1 0.14 0 0
CUI: C0475732
Disease: Hypercalcemia, Infantile
Hypercalcemia, Infantile 		5 0 1 0.14 0 0
CUI: C1833324
Disease: Sparse bone trabeculae
Sparse bone trabeculae 		5 0 1 0.14 0 0
CUI: C1833329
Disease: Bulging epiphyses
Bulging epiphyses 		5 0 1 0.14 0 0
CUI: C3715128
Disease: HYPOCALCEMIA, AUTOSOMAL DOMINANT 1
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1 		5 0 1 0.14 0 0