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: C4310473
Disease: Hypercalcemia, infantile, 2
Hypercalcemia, infantile, 2 		2 0 2 1.00 0 0
CUI: C0268080
Disease: Hypercalcemia, Idiopathic, of Infancy
Hypercalcemia, Idiopathic, of Infancy 		3 0 2 0.67 0 0
CUI: C0475733
Disease: Idiopathic infantile hypercalcemia - mild form
Idiopathic infantile hypercalcemia - mild form 		1 0 1 0.50 0 0
CUI: C2676786
Disease: Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1
Nephrolithiasis-Osteoporosis, Hypophosphatemic, 1 		1 0 1 0.50 0 0
CUI: C3150652
Disease: FANCONI RENOTUBULAR SYNDROME 2
FANCONI RENOTUBULAR SYNDROME 2 		1 0 1 0.50 0 0
CUI: C0475732
Disease: Hypercalcemia, Infantile
Hypercalcemia, Infantile 		5 0 2 0.40 0 0
CUI: C4551503
Disease: FANCONI RENOTUBULAR SYNDROME 1
FANCONI RENOTUBULAR SYNDROME 1 		2 0 1 0.33 0 0
CUI: C0948680
Disease: Adenocarcinoma of liver
Adenocarcinoma of liver 		3 0 1 0.25 0 0
CUI: C1853271
Disease: HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY
HYPOPHOSPHATEMIC RICKETS WITH HYPERCALCIURIA, HEREDITARY 		3 0 1 0.25 0 0
CUI: C0342951
Disease: Hypervitaminosis
Hypervitaminosis 		4 0 1 0.20 0 0
CUI: C0410445
Disease: Osteomalacia secondary to drug
Osteomalacia secondary to drug 		4 0 1 0.20 0 0
CUI: C0006705
Disease: Calcium Metabolism Disorders
Calcium Metabolism Disorders 		5 1 1 0.17 1 1.0E-01
CUI: C0342749
Disease: GLYCOGEN STORAGE DISEASE Ic
GLYCOGEN STORAGE DISEASE Ic 		5 0 1 0.17 0 0
CUI: C4087411
Disease: Oncogenic hypophosphataemic osteomalacia
Oncogenic hypophosphataemic osteomalacia 		5 0 1 0.17 0 0
CUI: C0026141
Disease: Milk-Alkali Syndrome
Milk-Alkali Syndrome 		13 0 2 0.15 0 0
CUI: C2363065
Disease: Vitamin D-resistant rickets
Vitamin D-resistant rickets 		6 0 1 0.14 0 0
CUI: C1833667
Disease: Elevated alkaline phosphatase of bone origin
Elevated alkaline phosphatase of bone origin 		7 0 1 0.12 0 0
CUI: C1845169
Disease: Renal phosphate wasting
Renal phosphate wasting 		8 0 1 0.11 0 0
CUI: C0403477
Disease: Medullary nephrocalcinosis
Medullary nephrocalcinosis 		9 0 1 1.0E-01 0 0
CUI: C0202178
Disease: Phosphorus measurement
Phosphorus measurement 		11 0 1 8.3E-02 0 0
CUI: C0332606
Disease: Elfin facies
Elfin facies 		11 0 1 8.3E-02 0 0
CUI: C0342642
Disease: Autosomal dominant hypophosphatemic rickets
Autosomal dominant hypophosphatemic rickets 		11 0 1 8.3E-02 0 0
CUI: C0523827
Disease: Inorganic phosphate measurement
Inorganic phosphate measurement 		11 0 1 8.3E-02 0 0
CUI: C1847868
Disease: Generalized aminoaciduria
Generalized aminoaciduria 		11 0 1 8.3E-02 0 0
CUI: C0032827
Disease: Potassium Deficiency
Potassium Deficiency 		14 0 1 6.7E-02 0 0