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: C4021572
Disease: Excessive wrinkling of palmar skin
Excessive wrinkling of palmar skin 		2 0 1 6.7E-02 0 0
CUI: C4310232
Disease: Hypercalcemia, Infantile, 1
Hypercalcemia, Infantile, 1 		2 0 1 6.7E-02 0 0
CUI: C4310473
Disease: Hypercalcemia, infantile, 2
Hypercalcemia, infantile, 2 		2 0 1 6.7E-02 0 0
CUI: C0008033
Disease: Pleuritic pain
Pleuritic pain 		3 0 1 6.2E-02 0 0
CUI: C0202100
Disease: Insulin C-peptide measurement
Insulin C-peptide measurement 		3 0 1 6.2E-02 0 0
CUI: C0266324
Disease: Congenital dilatation of ureter
Congenital dilatation of ureter 		3 0 1 6.2E-02 0 0
CUI: C0268080
Disease: Hypercalcemia, Idiopathic, of Infancy
Hypercalcemia, Idiopathic, of Infancy 		3 0 1 6.2E-02 0 0
CUI: C0271865
Disease: Autoimmune hypoparathyroidism
Autoimmune hypoparathyroidism 		3 0 1 6.2E-02 0 0
CUI: C0342634
Disease: Neonatal hypocalcemia
Neonatal hypocalcemia 		3 0 1 6.2E-02 0 0
CUI: C0403559
Disease: Dialysis disequilibrium syndrome
Dialysis disequilibrium syndrome 		3 0 1 6.2E-02 0 0
CUI: C0948680
Disease: Adenocarcinoma of liver
Adenocarcinoma of liver 		3 0 1 6.2E-02 0 0
CUI: C0036836
Disease: Serum total protein measurement
Serum total protein measurement 		4 0 1 5.9E-02 0 0
CUI: C0342951
Disease: Hypervitaminosis
Hypervitaminosis 		4 0 1 5.9E-02 0 0
CUI: C0410445
Disease: Osteomalacia secondary to drug
Osteomalacia secondary to drug 		4 0 1 5.9E-02 0 0
CUI: C1838440
Disease: ICHTHYOSIS EXFOLIATIVA
ICHTHYOSIS EXFOLIATIVA 		4 0 1 5.9E-02 0 0
CUI: C1853354
Disease: Peeling skin syndrome, acral type
Peeling skin syndrome, acral type 		4 0 1 5.9E-02 0 0
CUI: C1859115
Disease: Prominent interphalangeal joints
Prominent interphalangeal joints 		4 0 1 5.9E-02 0 0
CUI: C2750234
Disease: Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2
Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 		4 0 1 5.9E-02 0 0
CUI: C2930941
Disease: Carrington syndrome
Carrington syndrome 		4 0 1 5.9E-02 0 0
CUI: C0475732
Disease: Hypercalcemia, Infantile
Hypercalcemia, Infantile 		5 0 1 5.6E-02 0 0
CUI: C1295176
Disease: Leptin measurement
Leptin measurement 		5 0 1 5.6E-02 0 0
CUI: C1833372
Disease: HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III
HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL, TYPE III 		5 0 1 5.6E-02 0 0
CUI: C3715128
Disease: HYPOCALCEMIA, AUTOSOMAL DOMINANT 1
HYPOCALCEMIA, AUTOSOMAL DOMINANT 1 		5 0 1 5.6E-02 0 0
CUI: C3875492
Disease: Hypocalciuric hypercalcemia
Hypocalciuric hypercalcemia 		5 0 1 5.6E-02 0 0
CUI: C4073145
Disease: Hyperkeratosis pilaris
Hyperkeratosis pilaris 		5 0 1 5.6E-02 0 0