Source: ALL
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: C0015396
Disease: Eye Color
Eye Color 		13 0 2 4.7E-02 0 0
CUI: C0235971
Disease: Elevated alpha-fetoprotein
Elevated alpha-fetoprotein 		14 0 2 4.5E-02 0 0
CUI: C0334424
Disease: Nodular melanoma
Nodular melanoma 		15 0 2 4.4E-02 0 0
CUI: C0264122
Disease: Atrophy, Disuse
Atrophy, Disuse 		16 0 2 4.3E-02 0 0
CUI: C2242776
Disease: Plexiform leiomyoma
Plexiform leiomyoma 		41 0 3 4.3E-02 0 0
CUI: C0153943
Disease: Benign neoplasm of stomach
Benign neoplasm of stomach 		17 0 2 4.3E-02 0 0
CUI: C0496905
Disease: Neoplasm of uncertain or unknown behavior of stomach
Neoplasm of uncertain or unknown behavior of stomach 		17 0 2 4.3E-02 0 0
CUI: C0029131
Disease: Abnormality of the optic nerve
Abnormality of the optic nerve 		18 0 2 4.2E-02 0 0
CUI: C1536221
Disease: Non ST segment elevation myocardial infarction
Non ST segment elevation myocardial infarction 		18 0 2 4.2E-02 0 0
CUI: C0151891
Disease: Retinal depigmentation
Retinal depigmentation 		19 0 2 4.1E-02 0 0
CUI: C0154060
Disease: Carcinoma in situ of stomach
Carcinoma in situ of stomach 		19 0 2 4.1E-02 0 0
CUI: C0016689
Disease: Freckles
Freckles 		45 0 3 4.1E-02 0 0
CUI: C0677776
Disease: Hereditary Breast and Ovarian Cancer Syndrome
Hereditary Breast and Ovarian Cancer Syndrome 		74 0 4 3.9E-02 0 0
CUI: C1333991
Disease: Hereditary Non-Polyposis Colon Cancer Type 2
Hereditary Non-Polyposis Colon Cancer Type 2 		23 0 2 3.8E-02 0 0
CUI: C3278401
Disease: Hypopigmentation of hair
Hypopigmentation of hair 		23 0 2 3.8E-02 0 0
CUI: C0007117
Disease: Basal cell carcinoma
Basal cell carcinoma 		108 0 5 3.7E-02 0 0
CUI: C0349532
Disease: Gastric lymphoma
Gastric lymphoma 		24 0 2 3.7E-02 0 0
CUI: C1533041
Disease: Primary congenital glaucoma
Primary congenital glaucoma 		24 0 2 3.7E-02 0 0
CUI: C2936783
Disease: Colorectal cancer, hereditary nonpolyposis, type 1
Colorectal cancer, hereditary nonpolyposis, type 1 		24 0 2 3.7E-02 0 0
CUI: C2673946
Disease: Foveal hypoplasia (finding)
Foveal hypoplasia (finding) 		25 0 2 3.6E-02 0 0
CUI: C0005910
Disease: Body Weight
Body Weight 		57 0 3 3.5E-02 0 0
CUI: C0578626
Disease: blue iris (physical finding)
blue iris (physical finding) 		28 0 2 3.4E-02 0 0
CUI: C1368275
Disease: Pigmented Basal Cell Carcinoma
Pigmented Basal Cell Carcinoma 		28 0 2 3.4E-02 0 0
CUI: C4025756
Disease: Abnormal aortic morphology
Abnormal aortic morphology 		29 0 2 3.4E-02 0 0
CUI: C1456781
Disease: Benign melanocytic nevus
Benign melanocytic nevus 		122 0 5 3.4E-02 0 0