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: C1449844
Disease: Pseudohypoaldosteronism, Type II
Pseudohypoaldosteronism, Type II 		27 0 12 0.40 0 0
CUI: C1862472
Disease: Oculomelic amyoplasia
Oculomelic amyoplasia 		4 11 4 0.27 2 0.17
CUI: C0033805
Disease: Pseudohypoaldosteronism
Pseudohypoaldosteronism 		19 0 7 0.26 0 0
CUI: C4288936
Disease: Hyperkalemic Mineralocorticoid Resistance
Hyperkalemic Mineralocorticoid Resistance 		22 0 7 0.23 0 0
CUI: C0085679
Disease: Hyperchloremia
Hyperchloremia 		12 0 5 0.23 0 0
CUI: C1449842
Disease: Pseudohypoaldosteronism, Type I, Autosomal Dominant
Pseudohypoaldosteronism, Type I, Autosomal Dominant 		13 0 5 0.22 0 0
CUI: C3469605
Disease: PSEUDOHYPOALDOSTERONISM, TYPE IID
PSEUDOHYPOALDOSTERONISM, TYPE IID 		13 0 5 0.22 0 0
CUI: C1969073
Disease: Hyperchloremic metabolic acidosis
Hyperchloremic metabolic acidosis 		8 0 4 0.21 0 0
CUI: C1836756
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 4 (disorder)
ARTHROGRYPOSIS, DISTAL, TYPE 4 (disorder) 		3 0 3 0.20 0 0
CUI: C1852597
Disease: Arthrogryposis, distal, type 2E
Arthrogryposis, distal, type 2E 		3 0 3 0.20 0 0
CUI: C1861238
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 10
ARTHROGRYPOSIS, DISTAL, TYPE 10 		3 0 3 0.20 0 0
CUI: C1862471
Disease: Arthrogryposis-like hand anomaly and sensorineural deafness
Arthrogryposis-like hand anomaly and sensorineural deafness 		3 0 3 0.20 0 0
CUI: C3554415
Disease: Distal arthrogryposis type 5D
Distal arthrogryposis type 5D 		3 0 3 0.20 0 0
CUI: C3280526
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 1B
ARTHROGRYPOSIS, DISTAL, TYPE 1B 		4 0 3 0.19 0 0
CUI: C0265226
Disease: Hecht syndrome (disorder)
Hecht syndrome (disorder) 		5 0 3 0.18 0 0
CUI: C0268436
Disease: Pseudohypoaldosteronism, Type I
Pseudohypoaldosteronism, Type I 		19 0 5 0.17 0 0
CUI: C0220662
Disease: ARTHROGRYPOSIS, DISTAL, TYPE 1
ARTHROGRYPOSIS, DISTAL, TYPE 1 		9 0 3 0.14 0 0
CUI: C1846343
Disease: Bartter syndrome, type 3
Bartter syndrome, type 3 		9 0 3 0.14 0 0
CUI: C0085570
Disease: Hypokalemic alkalosis
Hypokalemic alkalosis 		10 0 3 0.14 0 0
CUI: C0740898
Disease: Hypokalemic metabolic alkalosis
Hypokalemic metabolic alkalosis 		10 0 3 0.14 0 0
CUI: C1449843
Disease: Pseudohypoaldosteronism, Type I, Autosomal Recessive
Pseudohypoaldosteronism, Type I, Autosomal Recessive 		10 0 3 0.14 0 0
CUI: C2713447
Disease: Hyperpotassemia and Hypertension, Familial
Hyperpotassemia and Hypertension, Familial 		10 0 3 0.14 0 0
CUI: C1862479
Disease: Absent phalangeal crease
Absent phalangeal crease 		3 0 2 0.12 0 0
CUI: C0265213
Disease: Distal arthrogryposis syndrome
Distal arthrogryposis syndrome 		22 0 4 0.12 0 0
CUI: C0271728
Disease: Secondary hyperaldosteronism
Secondary hyperaldosteronism 		4 0 2 0.12 0 0