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: C1334386
Disease: Meningeal melanoma
Meningeal melanoma
23 0 10 8.8E-02 0 0
CUI: C0162283
Disease: Nephrogenic Diabetes Insipidus
Nephrogenic Diabetes Insipidus
60 0 13 8.8E-02 0 0
CUI: C0597854
Disease: renin induced hypertension
renin induced hypertension
11 0 9 8.8E-02 0 0
CUI: C1809471
Disease: Familial benign hypercalcemia
Familial benign hypercalcemia
24 0 10 8.8E-02 0 0
Postural Orthostatic Tachycardia Syndrome
25 0 10 8.7E-02 0 0
CUI: C0018378
Disease: Guillain-Barre Syndrome
Guillain-Barre Syndrome
163 0 21 8.7E-02 0 0
CUI: C0343723
Disease: Neonatal chlamydial conjunctivitis
Neonatal chlamydial conjunctivitis
38 0 11 8.7E-02 0 0
CUI: C0162820
Disease: Dermatitis, Allergic Contact
Dermatitis, Allergic Contact
151 0 20 8.7E-02 0 0
CUI: C0023891
Disease: Liver Cirrhosis, Alcoholic
Liver Cirrhosis, Alcoholic
126 15 18 8.7E-02 1 2.6E-02
CUI: C3279470
Disease: HYPOTRICHOSIS 8
HYPOTRICHOSIS 8
13 0 9 8.7E-02 0 0
CUI: C0008350
Disease: Cholelithiasis
Cholelithiasis
252 90 28 8.6E-02 3 2.7E-02
CUI: C0019340
Disease: Herpes NOS
Herpes NOS
114 0 17 8.6E-02 0 0
CUI: C0040592
Disease: Trachoma
Trachoma
39 0 11 8.6E-02 0 0
Enteropathy-Associated T-Cell Lymphoma
39 0 11 8.6E-02 0 0
CUI: C0010418
Disease: Cryptosporidiosis
Cryptosporidiosis
40 0 11 8.5E-02 0 0
CUI: C0019100
Disease: Severe Dengue
Severe Dengue
117 0 17 8.5E-02 0 0
CUI: C0745744
Disease: End Stage Liver Disease
End Stage Liver Disease
80 3 14 8.4E-02 1 3.8E-02
CUI: C0023646
Disease: Lichen Planus
Lichen Planus
106 0 16 8.4E-02 0 0
CUI: C4048195
Disease: Autosomal dominant hypocalcemia
Autosomal dominant hypocalcemia
29 0 10 8.4E-02 0 0
Aggressive periodontitis, generalized
56 0 12 8.3E-02 0 0
CUI: C0016382
Disease: Flushing
Flushing
83 0 14 8.3E-02 0 0
CUI: C0039263
Disease: Takayasu Arteritis
Takayasu Arteritis
136 0 18 8.3E-02 0 0
CUI: C0860603
Disease: Anxiety symptoms
Anxiety symptoms
110 0 16 8.2E-02 0 0
CUI: C0268307
Disease: Conjugated hyperbilirubinemia
Conjugated hyperbilirubinemia
32 0 10 8.2E-02 0 0
CUI: C1704321
Disease: Nephrotic Syndrome, Minimal Change
Nephrotic Syndrome, Minimal Change
85 0 14 8.2E-02 0 0