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: C4288936
Disease: Hyperkalemic Mineralocorticoid Resistance
Hyperkalemic Mineralocorticoid Resistance 		22 3 15 0.44 3 7.1E-02
CUI: C0033805
Disease: Pseudohypoaldosteronism
Pseudohypoaldosteronism 		19 0 14 0.44 0 0
CUI: C1449842
Disease: Pseudohypoaldosteronism, Type I, Autosomal Dominant
Pseudohypoaldosteronism, Type I, Autosomal Dominant 		13 0 12 0.43 0 0
CUI: C0220666
Disease: ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA
ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE IIA 		15 0 12 0.40 0 0
CUI: C1449843
Disease: Pseudohypoaldosteronism, Type I, Autosomal Recessive
Pseudohypoaldosteronism, Type I, Autosomal Recessive 		10 0 10 0.37 0 0
CUI: C2713447
Disease: Hyperpotassemia and Hypertension, Familial
Hyperpotassemia and Hypertension, Familial 		10 0 10 0.37 0 0
CUI: C0268436
Disease: Pseudohypoaldosteronism, Type I
Pseudohypoaldosteronism, Type I 		19 0 12 0.35 0 0
CUI: C0221043
Disease: Liddle Syndrome
Liddle Syndrome 		19 0 8 0.21 0 0
CUI: C0085679
Disease: Hyperchloremia
Hyperchloremia 		12 0 6 0.18 0 0
CUI: C3469605
Disease: PSEUDOHYPOALDOSTERONISM, TYPE IID
PSEUDOHYPOALDOSTERONISM, TYPE IID 		13 29 6 0.18 22 0.45
CUI: C1846345
Disease: Hyperactive renin-angiotensin system
Hyperactive renin-angiotensin system 		8 0 5 0.17 0 0
CUI: C0020461
Disease: Hyperkalemia
Hyperkalemia 		32 0 8 0.16 0 0
CUI: C0220983
Disease: Metabolic alkalosis
Metabolic alkalosis 		27 0 7 0.15 0 0
CUI: C0030779
Disease: Pelger-Huet Anomaly
Pelger-Huet Anomaly 		25 0 6 0.13 0 0
CUI: C1969073
Disease: Hyperchloremic metabolic acidosis
Hyperchloremic metabolic acidosis 		8 0 4 0.13 0 0
CUI: C0085570
Disease: Hypokalemic alkalosis
Hypokalemic alkalosis 		10 0 4 0.12 0 0
CUI: C1864105
Disease: Low urinary cyclic AMP response to PTH administration
Low urinary cyclic AMP response to PTH administration 		3 0 3 0.11 0 0
CUI: C0268450
Disease: Gitelman Syndrome
Gitelman Syndrome 		26 0 5 0.10 0 0
CUI: C1859569
Disease: BARDET-BIEDL SYNDROME 11
BARDET-BIEDL SYNDROME 11 		5 0 3 0.10 0 0
CUI: C0524582
Disease: Mulibrey Nanism
Mulibrey Nanism 		7 0 3 9.7E-02 0 0
CUI: C0795858
Disease: Chromosome 15q, trisomy
Chromosome 15q, trisomy 		7 0 3 9.7E-02 0 0
CUI: C4023112
Disease: Acute infectious pneumonia
Acute infectious pneumonia 		7 0 3 9.7E-02 0 0
CUI: C4025204
Disease: Recurrent Haemophilus influenzae infections
Recurrent Haemophilus influenzae infections 		7 0 3 9.7E-02 0 0
CUI: C0342488
Disease: Mineralocorticoid Excess Syndrome, Apparent
Mineralocorticoid Excess Syndrome, Apparent 		8 0 3 9.4E-02 0 0
CUI: C1859305
Disease: Cerebellar Ataxia and Hypogonadotropic Hypogonadism
Cerebellar Ataxia and Hypogonadotropic Hypogonadism 		8 0 3 9.4E-02 0 0