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: C1322252
Disease: Chordoid Glioma of the Third Ventricle
Chordoid Glioma of the Third Ventricle 		2 0 1 0.25 0 0
CUI: C2985174
Disease: Papillary glioneuronal tumor
Papillary glioneuronal tumor 		2 0 1 0.25 0 0
CUI: C0268443
Disease: Acquired Nephrogenic Diabetes Insipidus
Acquired Nephrogenic Diabetes Insipidus 		3 0 1 0.20 0 0
CUI: C1563706
Disease: Nephrogenic Diabetes Insipidus, Type II
Nephrogenic Diabetes Insipidus, Type II 		3 0 1 0.20 0 0
CUI: C3542500
Disease: ADH-Resistant Diabetes Insipidus
ADH-Resistant Diabetes Insipidus 		3 0 1 0.20 0 0
CUI: C0853104
Disease: Renal tubular atrophy
Renal tubular atrophy 		4 0 1 0.17 0 0
CUI: C1302746
Disease: Melanocytic neoplasm
Melanocytic neoplasm 		4 0 1 0.17 0 0
CUI: C1865926
Disease: Infantile convulsions and paroxysmal choreoathetosis, familial (disorder)
Infantile convulsions and paroxysmal choreoathetosis, familial (disorder) 		4 0 1 0.17 0 0
CUI: C1854181
Disease: FIBROMATOSIS, GINGIVAL, 2
FIBROMATOSIS, GINGIVAL, 2 		6 0 1 0.12 0 0
CUI: C4021885
Disease: Atrial cardiomyopathy
Atrial cardiomyopathy 		7 0 1 0.11 0 0
CUI: C0332886
Disease: Coarctation
Coarctation 		8 0 1 1.0E-01 0 0
CUI: C1834304
Disease: AMYOTROPHY, HEREDITARY NEURALGIC
AMYOTROPHY, HEREDITARY NEURALGIC 		9 0 1 9.1E-02 0 0
CUI: C0523953
Disease: Cardiac troponin T measurement
Cardiac troponin T measurement 		11 0 1 7.7E-02 0 0
CUI: C0677501
Disease: Congenital Nephrogenic Diabetes Insipidus
Congenital Nephrogenic Diabetes Insipidus 		11 0 1 7.7E-02 0 0
CUI: C1333500
Disease: Extragastrointestinal Gastrointestinal Stromal Tumor
Extragastrointestinal Gastrointestinal Stromal Tumor 		12 0 1 7.1E-02 0 0
CUI: C2721670
Disease: Ultrafiltration failure
Ultrafiltration failure 		12 0 1 7.1E-02 0 0
CUI: C3888552
Disease: Autoimmune colitis
Autoimmune colitis 		12 0 1 7.1E-02 0 0
CUI: C1853230
Disease: Aphakia, congenital primary
Aphakia, congenital primary 		14 0 1 6.2E-02 0 0
CUI: C1719788
Disease: Episodic ataxia type 1
Episodic ataxia type 1 		16 0 1 5.6E-02 0 0
CUI: C0018803
Disease: Heart Function Tests
Heart Function Tests 		17 0 1 5.3E-02 0 0
CUI: C4085595
Disease: AL-RAQAD SYNDROME
AL-RAQAD SYNDROME 		17 0 1 5.3E-02 0 0
CUI: C0741281
Disease: atrial fibrillation new onset
atrial fibrillation new onset 		18 0 1 5.0E-02 0 0
CUI: C0267176
Disease: Gastroparesis with diabetes mellitus
Gastroparesis with diabetes mellitus 		21 0 1 4.3E-02 0 0
CUI: C1861861
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder) 		21 0 1 4.3E-02 0 0
CUI: C0014236
Disease: Endophthalmitis
Endophthalmitis 		22 0 1 4.2E-02 0 0