Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Cerebral Palsy, Spastic Quadriplegic, 1
3 0 1 0.14 0 0
CUI: C3146249
Disease: Stage IV Renal Cell Cancer AJCC v7
Stage IV Renal Cell Cancer AJCC v7
3 0 1 0.14 0 0
CUI: C4288409
Disease: Perforin Deficiency
Perforin Deficiency
3 0 1 0.14 0 0
Eosinophilic meningitis due to Angiostrongylus cantonensis
3 0 1 0.14 0 0
Steroid Refractory Graft Versus Host Disease
3 0 1 0.14 0 0
CUI: C0153308
Disease: Toxoplasmosis chorioretinitis
Toxoplasmosis chorioretinitis
4 0 1 0.12 0 0
CUI: C0398701
Disease: Immunoglobulin G2 deficiency
Immunoglobulin G2 deficiency
4 0 1 0.12 0 0
CUI: C0862448
Disease: Stage IV Renal Cell Cancer
Stage IV Renal Cell Cancer
4 0 1 0.12 0 0
Secondary angle-closure glaucoma - synechial
4 0 1 0.12 0 0
CUI: C1282916
Disease: Secondary Raynaud's phenomenon
Secondary Raynaud's phenomenon
4 0 1 0.12 0 0
Interleukin 2 Receptor, Alpha, Deficiency of
4 0 1 0.12 0 0
CUI: C3152055
Disease: D-2-HYDROXYGLUTARIC ACIDURIA 1
D-2-HYDROXYGLUTARIC ACIDURIA 1
4 15 1 0.12 3 2.4E-02
CUI: C3160792
Disease: Lamellar macular hole
Lamellar macular hole
4 0 1 0.12 0 0
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2Q
4 0 1 0.12 0 0
CUI: C0154947
Disease: Anatomical narrow angle glaucoma
Anatomical narrow angle glaucoma
5 0 1 0.11 0 0
CUI: C0702159
Disease: Constitutional aplastic anemia
Constitutional aplastic anemia
5 0 1 0.11 0 0
Severe combined immunodeficiency, atypical
5 0 1 0.11 0 0
CUI: C3472600
Disease: Chronic hepatitis E
Chronic hepatitis E
5 0 1 0.11 0 0
CUI: C4025603
Disease: Glutaric acidemia
Glutaric acidemia
5 0 1 0.11 0 0
CUI: C0014324
Disease: Entamoebiasis
Entamoebiasis
6 0 1 1.0E-01 0 0
CUI: C0014858
Disease: Esophageal motility disorders
Esophageal motility disorders
6 0 1 1.0E-01 0 0
CUI: C0014863
Disease: Esophageal spasm
Esophageal spasm
6 0 1 1.0E-01 0 0
CUI: C0392998
Disease: Carcinosarcoma of ovary
Carcinosarcoma of ovary
6 0 1 1.0E-01 0 0
CUI: C0399368
Disease: Amelogenesis Imperfecta, Type IB
Amelogenesis Imperfecta, Type IB
6 0 1 1.0E-01 0 0
CUI: C0543687
Disease: Thymic alymphoplasia
Thymic alymphoplasia
6 0 1 1.0E-01 0 0