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: C4021028
Disease: Pseudo-fractures
Pseudo-fractures 		10 0 9 7.6E-02 0 0
CUI: C0029464
Disease: Osteosclerosis
Osteosclerosis 		82 0 14 7.5E-02 0 0
CUI: C0332606
Disease: Elfin facies
Elfin facies 		11 0 9 7.5E-02 0 0
CUI: C0268412
Disease: Infantile hypophosphatasia
Infantile hypophosphatasia 		12 0 9 7.4E-02 0 0
CUI: C0020630
Disease: Hypophosphatasia
Hypophosphatasia 		27 0 10 7.4E-02 0 0
CUI: C0035078
Disease: Kidney Failure
Kidney Failure 		378 0 34 7.4E-02 0 0
CUI: C1704375
Disease: Hypophosphatemic Rickets
Hypophosphatemic Rickets 		29 6 10 7.3E-02 1 4.0E-02
CUI: C0020599
Disease: Hypocalciuria
Hypocalciuria 		16 0 9 7.2E-02 0 0
CUI: C4022012
Disease: Death in early adulthood
Death in early adulthood 		46 0 11 7.2E-02 0 0
CUI: C0020621
Disease: Hypokalemia
Hypokalemia 		61 0 12 7.2E-02 0 0
CUI: C0085602
Disease: Polydipsia
Polydipsia 		61 0 12 7.2E-02 0 0
CUI: C0520739
Disease: Hereditary pyropoikilocytosis
Hereditary pyropoikilocytosis 		47 0 11 7.1E-02 0 0
CUI: C0042870
Disease: Vitamin D Deficiency
Vitamin D Deficiency 		153 0 18 7.1E-02 0 0
CUI: C0020598
Disease: Hypocalcemia
Hypocalcemia 		94 0 14 7.1E-02 0 0
CUI: C0041948
Disease: Uremia
Uremia 		110 0 15 7.0E-02 0 0
CUI: C1963165
Disease: Malabsorption, CTCAE
Malabsorption, CTCAE 		175 0 19 6.9E-02 0 0
CUI: C3714745
Disease: Malabsorption
Malabsorption 		175 0 19 6.9E-02 0 0
CUI: C4552839
Disease: Hypomagnesemia, CTCAE
Hypomagnesemia, CTCAE 		21 0 9 6.9E-02 0 0
CUI: C0020503
Disease: Hyperparathyroidism, Secondary
Hyperparathyroidism, Secondary 		68 0 12 6.9E-02 0 0
CUI: C0024523
Disease: Malabsorption Syndrome
Malabsorption Syndrome 		239 0 23 6.9E-02 0 0
CUI: C0033687
Disease: Proteinuria
Proteinuria 		239 0 23 6.9E-02 0 0
CUI: C0344529
Disease: Cornea plana
Cornea plana 		22 0 9 6.9E-02 0 0
CUI: C0003499
Disease: Supravalvular aortic stenosis
Supravalvular aortic stenosis 		23 0 9 6.8E-02 0 0
CUI: C4025732
Disease: Tubulointerstitial abnormality
Tubulointerstitial abnormality 		23 0 9 6.8E-02 0 0
CUI: C4024897
Disease: Atrophy/Degeneration involving the corticospinal tracts
Atrophy/Degeneration involving the corticospinal tracts 		8 0 8 6.8E-02 0 0