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: C0007166
Disease: Low Cardiac Output
Low Cardiac Output
1 0 1 1.00 0 0
CUI: C0600177
Disease: Low Cardiac Output Syndrome
Low Cardiac Output Syndrome
1 0 1 1.00 0 0
CUI: C0001122
Disease: Acidosis
Acidosis
2 0 1 0.50 0 0
CUI: C0220981
Disease: Metabolic acidosis
Metabolic acidosis
2 0 1 0.50 0 0
CUI: C0022593
Disease: Keratosis
Keratosis
5 0 1 0.20 0 0
CUI: C0022594
Disease: Keratosis Blennorrhagica
Keratosis Blennorrhagica
5 0 1 0.20 0 0
CUI: C0086501
Disease: Keratoma
Keratoma
5 0 1 0.20 0 0
Gonadotropin-Resistant Ovary Syndrome
6 0 1 0.17 0 0
CUI: C2718076
Disease: Fetal Mummification
Fetal Mummification
6 0 1 0.17 0 0
Hypergonadotropic Ovarian Failure, X-Linked
6 0 1 0.17 0 0
CUI: C4552079
Disease: Premature Ovarian Failure 1
Premature Ovarian Failure 1
6 0 1 0.17 0 0
Experimental Autoimmune Encephalomyelitis
9 0 1 0.11 0 0
CUI: C1306571
Disease: Hepatic Insufficiency
Hepatic Insufficiency
9 0 1 0.11 0 0
CUI: C0002895
Disease: Anemia, Sickle Cell
Anemia, Sickle Cell
10 0 1 1.0E-01 0 0
Pathological accumulation of air in tissues
12 0 1 8.3E-02 0 0
CUI: C0017178
Disease: Gastrointestinal Diseases
Gastrointestinal Diseases
12 0 1 8.3E-02 0 0
Functional Gastrointestinal Disorders
12 0 1 8.3E-02 0 0
CUI: C1565321
Disease: Cholera Infantum
Cholera Infantum
12 0 1 8.3E-02 0 0
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
13 0 1 7.7E-02 0 0
CUI: C0333704
Disease: Chromosome Breaks
Chromosome Breaks
14 0 1 7.1E-02 0 0
CUI: C0376628
Disease: Chromosome Breakage
Chromosome Breakage
14 0 1 7.1E-02 0 0
CUI: C0042900
Disease: Vitiligo
Vitiligo
17 0 1 5.9E-02 0 0
CUI: C0085215
Disease: Ovarian Failure, Premature
Ovarian Failure, Premature
21 0 1 4.8E-02 0 0
CUI: C0600519
Disease: Ventricular Remodeling
Ventricular Remodeling
21 0 1 4.8E-02 0 0
CUI: C0600520
Disease: Left Ventricle Remodeling
Left Ventricle Remodeling
21 0 1 4.8E-02 0 0