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: C1846343
Disease: Bartter syndrome, type 3
Bartter syndrome, type 3
9 0 3 6.4E-02 0 0
CUI: C0268495
Disease: Oculocutaneous albinism type 2
Oculocutaneous albinism type 2
11 0 3 6.1E-02 0 0
CUI: C1959588
Disease: Angioma
Angioma
11 0 3 6.1E-02 0 0
Congenital cytomegalovirus infection
29 0 4 6.1E-02 0 0
CUI: C0029877
Disease: Ear Inflammation
Ear Inflammation
12 0 3 6.0E-02 0 0
CUI: C0751699
Disease: Minimally Conscious State
Minimally Conscious State
12 0 3 6.0E-02 0 0
CUI: C0085581
Disease: Restrictive lung disease
Restrictive lung disease
13 0 3 5.9E-02 0 0
CUI: C0080024
Disease: Piebaldism
Piebaldism
33 0 4 5.7E-02 0 0
CUI: C0220724
Disease: CONSTRICTING BANDS, CONGENITAL
CONSTRICTING BANDS, CONGENITAL
16 0 3 5.6E-02 0 0
CUI: C0699744
Disease: Infection of ear
Infection of ear
16 0 3 5.6E-02 0 0
CUI: C1838625
Disease: Warburg Sjo Fledelius syndrome
Warburg Sjo Fledelius syndrome
16 0 3 5.6E-02 0 0
CUI: C0751074
Disease: Diabetic Neuralgia
Diabetic Neuralgia
36 0 4 5.5E-02 0 0
CUI: C0154920
Disease: Pigmentary iris degeneration
Pigmentary iris degeneration
37 0 4 5.4E-02 0 0
CUI: C0267375
Disease: Chronic colitis
Chronic colitis
57 0 5 5.4E-02 0 0
CUI: C0030443
Disease: Familial Periodic Paralysis
Familial Periodic Paralysis
18 0 3 5.4E-02 0 0
CUI: C0205788
Disease: Histiocytoid hemangioma
Histiocytoid hemangioma
18 0 3 5.4E-02 0 0
CUI: C0740985
Disease: Acute anaemia
Acute anaemia
18 0 3 5.4E-02 0 0
CUI: C1279412
Disease: periodic paralysis (finding)
periodic paralysis (finding)
18 0 3 5.4E-02 0 0
CUI: C4704753
Disease: Urinary Bladder, Underactive
Urinary Bladder, Underactive
20 0 3 5.2E-02 0 0
CUI: C0008525
Disease: Choroideremia
Choroideremia
41 0 4 5.1E-02 0 0
Gastroparesis with diabetes mellitus
21 0 3 5.1E-02 0 0
CUI: C0549493
Disease: Alveolitis
Alveolitis
63 0 5 5.1E-02 0 0
CUI: C2826321
Disease: Refractory Thrombocytopenia
Refractory Thrombocytopenia
22 0 3 5.0E-02 0 0
CUI: C0751951
Disease: Central Core Myopathy (disorder)
Central Core Myopathy (disorder)
44 0 4 4.9E-02 0 0
CUI: C1739395
Disease: Takotsubo Cardiomyopathy
Takotsubo Cardiomyopathy
44 0 4 4.9E-02 0 0