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: C0015190
Disease: Euthyroid Sick Syndromes
Euthyroid Sick Syndromes
1 1 1 0.11 1 9.1E-02
CUI: C0019825
Disease: Hoarseness
Hoarseness
1 1 1 0.11 1 9.1E-02
CUI: C0021141
Disease: Inappropriate ADH Syndrome
Inappropriate ADH Syndrome
1 1 1 0.11 1 9.1E-02
CUI: C0021933
Disease: Intussusception
Intussusception
1 1 1 0.11 1 9.1E-02
CUI: C0025467
Disease: Mesenteric Cyst
Mesenteric Cyst
1 2 1 0.11 2 0.18
CUI: C0029423
Disease: Cartilaginous exostosis
Cartilaginous exostosis
1 2 1 0.11 2 0.18
CUI: C0030446
Disease: Paralytic Ileus
Paralytic Ileus
1 1 1 0.11 1 9.1E-02
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
1 74 1 0.11 1 1.2E-02
CUI: C0035232
Disease: Respiratory Paralysis
Respiratory Paralysis
1 1 1 0.11 1 9.1E-02
CUI: C0042138
Disease: Uterine Neoplasms
Uterine Neoplasms
1 1 1 0.11 1 9.1E-02
CUI: C0085417
Disease: Epilepsy, Complex Partial
Epilepsy, Complex Partial
1 0 1 0.11 0 0
CUI: C0085637
Disease: Oculogyric crisis
Oculogyric crisis
1 0 1 0.11 0 0
CUI: C0162565
Disease: Acute intermittent porphyria
Acute intermittent porphyria
1 39 1 0.11 1 2.0E-02
CUI: C0206619
Disease: Lymphatic Vessel Tumors
Lymphatic Vessel Tumors
1 2 1 0.11 2 0.18
CUI: C0239846
Disease: Hand-wringing
Hand-wringing
1 0 1 0.11 0 0
CUI: C0270971
Disease: Floppy infant syndrome
Floppy infant syndrome
1 0 1 0.11 0 0
CUI: C0338614
Disease: Psychotic episodes
Psychotic episodes
1 1 1 0.11 1 9.1E-02
Hereditary C1 esterase inhibitor deficiency - dysfunctional factor
1 0 1 0.11 0 0
CUI: C0425492
Disease: Irregular breathing
Irregular breathing
1 0 1 0.11 0 0
CUI: C0554980
Disease: Moody (finding)
Moody (finding)
1 1 1 0.11 1 9.1E-02
CUI: C0740394
Disease: Hyperuricemia
Hyperuricemia
1 1 1 0.11 1 9.1E-02
CUI: C1142132
Disease: Carnitine deficiency
Carnitine deficiency
1 0 1 0.11 0 0
CUI: C1142277
Disease: Brown urine
Brown urine
1 1 1 0.11 1 9.1E-02
CUI: C1608410
Disease: Head titubation
Head titubation
1 0 1 0.11 0 0
CUI: C1832466
Disease: CAPOS syndrome
CAPOS syndrome
1 10 1 0.11 1 5.0E-02