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: C0853277
Disease: Pseudo-Bartter syndrome
Pseudo-Bartter syndrome 		2 0 1 4.2E-02 0 0
CUI: C0865171
Disease: parathyroiditis
parathyroiditis 		2 0 1 4.2E-02 0 0
CUI: C0995195
Disease: Anoxia of brain
Anoxia of brain 		2 0 1 4.2E-02 0 0
CUI: C1140716
Disease: Hypoxic Brain Damage
Hypoxic Brain Damage 		2 0 1 4.2E-02 0 0
CUI: C1446787
Disease: Cramping sensation quality
Cramping sensation quality 		2 0 1 4.2E-02 0 0
CUI: C1845837
Disease: Dyserythropoietic Anemia with Thrombocytopenia
Dyserythropoietic Anemia with Thrombocytopenia 		2 0 1 4.2E-02 0 0
CUI: C1857788
Disease: Atrophy of the dentate nucleus
Atrophy of the dentate nucleus 		2 0 1 4.2E-02 0 0
CUI: C3150215
Disease: CHROMOSOME 6q24-q25 DELETION SYNDROME
CHROMOSOME 6q24-q25 DELETION SYNDROME 		2 0 1 4.2E-02 0 0
CUI: C3807541
Disease: MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY
MACROCEPHALY AND EPILEPTIC ENCEPHALOPATHY 		2 0 1 4.2E-02 0 0
CUI: C4021572
Disease: Excessive wrinkling of palmar skin
Excessive wrinkling of palmar skin 		2 0 1 4.2E-02 0 0
CUI: C4310232
Disease: Hypercalcemia, Infantile, 1
Hypercalcemia, Infantile, 1 		2 0 1 4.2E-02 0 0
CUI: C4310473
Disease: Hypercalcemia, infantile, 2
Hypercalcemia, infantile, 2 		2 0 1 4.2E-02 0 0
CUI: C0008033
Disease: Pleuritic pain
Pleuritic pain 		3 0 1 4.0E-02 0 0
CUI: C0202100
Disease: Insulin C-peptide measurement
Insulin C-peptide measurement 		3 0 1 4.0E-02 0 0
CUI: C0266324
Disease: Congenital dilatation of ureter
Congenital dilatation of ureter 		3 0 1 4.0E-02 0 0
CUI: C0268080
Disease: Hypercalcemia, Idiopathic, of Infancy
Hypercalcemia, Idiopathic, of Infancy 		3 0 1 4.0E-02 0 0
CUI: C0271865
Disease: Autoimmune hypoparathyroidism
Autoimmune hypoparathyroidism 		3 0 1 4.0E-02 0 0
CUI: C0342634
Disease: Neonatal hypocalcemia
Neonatal hypocalcemia 		3 0 1 4.0E-02 0 0
CUI: C0393933
Disease: Pseudomyopathic myasthenia
Pseudomyopathic myasthenia 		3 0 1 4.0E-02 0 0
CUI: C0403559
Disease: Dialysis disequilibrium syndrome
Dialysis disequilibrium syndrome 		3 0 1 4.0E-02 0 0
CUI: C0948680
Disease: Adenocarcinoma of liver
Adenocarcinoma of liver 		3 0 1 4.0E-02 0 0
CUI: C1303009
Disease: Microcoria, congenital
Microcoria, congenital 		3 0 1 4.0E-02 0 0
CUI: C1850792
Disease: Congenital myasthenic syndrome ib
Congenital myasthenic syndrome ib 		3 0 1 4.0E-02 0 0
CUI: C1861451
Disease: Stormorken Syndrome
Stormorken Syndrome 		3 0 1 4.0E-02 0 0
CUI: C2748557
Disease: Immune dysfunction with T-cell inactivation due to calcium entry defect 2
Immune dysfunction with T-cell inactivation due to calcium entry defect 2 		3 0 1 4.0E-02 0 0