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: C0009398
Disease: Color vision defect
Color vision defect
0 4 0 0 2 3.6E-02
CUI: C0152115
Disease: Lingual-Facial-Buccal Dyskinesia
Lingual-Facial-Buccal Dyskinesia
0 4 0 0 1 1.8E-02
CUI: C0948392
Disease: Borderline mental impairment
Borderline mental impairment
0 1 0 0 1 1.9E-02
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy
0 9 0 0 1 1.6E-02
CUI: C4694057
Disease: Taq1A POLYMORPHISM
Taq1A POLYMORPHISM
0 14 0 0 2 3.0E-02
CUI: C0854723
Disease: Retinal Dystrophies
Retinal Dystrophies
113 0 1 2.9E-03 0 0
CUI: C0266999
Disease: Vesicular Stomatitis
Vesicular Stomatitis
107 0 1 3.0E-03 0 0
CUI: C4552100
Disease: Lynch Syndrome
Lynch Syndrome
102 0 1 3.0E-03 0 0
CUI: C0686353
Disease: Muscular Dystrophies, Limb-Girdle
Muscular Dystrophies, Limb-Girdle
100 0 1 3.1E-03 0 0
CUI: C0149939
Disease: Obstructive nephropathy
Obstructive nephropathy
94 0 1 3.1E-03 0 0
CUI: C1847540
Disease: Azoospermia, Nonobstructive
Azoospermia, Nonobstructive
90 0 1 3.2E-03 0 0
CUI: C0016719
Disease: Friedreich Ataxia
Friedreich Ataxia
88 0 1 3.2E-03 0 0
CUI: C0584960
Disease: Factor V Leiden mutation
Factor V Leiden mutation
86 0 1 3.2E-03 0 0
Non-ST Elevated Myocardial Infarction
85 0 1 3.2E-03 0 0
Purpura, Thrombotic Thrombocytopenic
77 0 1 3.3E-03 0 0
CUI: C0206693
Disease: Medullary carcinoma
Medullary carcinoma
75 0 1 3.3E-03 0 0
CUI: C1334953
Disease: Neuroblastic tumors
Neuroblastic tumors
73 0 1 3.3E-03 0 0
CUI: C0339789
Disease: Congenital deafness
Congenital deafness
72 0 1 3.3E-03 0 0
CUI: C0235480
Disease: Paroxysmal atrial fibrillation
Paroxysmal atrial fibrillation
71 0 1 3.4E-03 0 0
Idiopathic hypogonadotropic hypogonadism
71 0 1 3.4E-03 0 0
CUI: C0031269
Disease: Peutz-Jeghers Syndrome
Peutz-Jeghers Syndrome
70 0 1 3.4E-03 0 0
CUI: C0276275
Disease: Disease due to Parvoviridae
Disease due to Parvoviridae
70 0 1 3.4E-03 0 0
CUI: C1859592
Disease: ATRICHIA WITH PAPULAR LESIONS
ATRICHIA WITH PAPULAR LESIONS
68 0 1 3.4E-03 0 0
CUI: C4551714
Disease: Rod-Cone Dystrophy
Rod-Cone Dystrophy
68 0 1 3.4E-03 0 0
CUI: C1861922
Disease: CAMPOMELIC DYSPLASIA
CAMPOMELIC DYSPLASIA
67 0 1 3.4E-03 0 0