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: C0334091
Disease: Biliary hamartoma
Biliary hamartoma 		2 0 2 0.12 0 0
CUI: C4551623
Disease: EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1
EHLERS-DANLOS SYNDROME, ARTHROCHALASIA TYPE, 1 		3 0 2 0.12 0 0
CUI: C0033587
Disease: Prosthesis Loosening
Prosthesis Loosening 		6 0 2 1.0E-01 0 0
CUI: C0432291
Disease: Mandibuloacral dysostosis
Mandibuloacral dysostosis 		17 0 3 1.0E-01 0 0
CUI: C1850625
Disease: Native American myopathy
Native American myopathy 		6 0 2 1.0E-01 0 0
CUI: C4317126
Disease: Niacin deficiency
Niacin deficiency 		7 0 2 9.5E-02 0 0
CUI: C0677950
Disease: Stage IV Colorectal Cancer
Stage IV Colorectal Cancer 		19 0 3 9.4E-02 0 0
CUI: C3146251
Disease: Stage IV Colorectal Cancer AJCC v7
Stage IV Colorectal Cancer AJCC v7 		19 0 3 9.4E-02 0 0
CUI: C0010631
Disease: Cystadenocarcinoma
Cystadenocarcinoma 		8 0 2 9.1E-02 0 0
CUI: C4049005
Disease: Cataract, total congenital with posterior sutural opacities in Heterozygotes
Cataract, total congenital with posterior sutural opacities in Heterozygotes 		8 0 2 9.1E-02 0 0
CUI: C0008309
Disease: Bile duct adenoma
Bile duct adenoma 		9 0 2 8.7E-02 0 0
CUI: C0011304
Disease: Demyelination
Demyelination 		9 0 2 8.7E-02 0 0
CUI: C0151773
Disease: Bone marrow depression
Bone marrow depression 		9 0 2 8.7E-02 0 0
CUI: C2350037
Disease: Clinically Isolated Syndrome, CNS Demyelinating
Clinically Isolated Syndrome, CNS Demyelinating 		9 0 2 8.7E-02 0 0
CUI: C2749515
Disease: Collapsing glomerulopathy
Collapsing glomerulopathy 		10 0 2 8.3E-02 0 0
CUI: C2930930
Disease: Abdominal obesity metabolic syndrome
Abdominal obesity metabolic syndrome 		10 0 2 8.3E-02 0 0
CUI: C0013930
Disease: Embolism, Tumor
Embolism, Tumor 		12 0 2 7.7E-02 0 0
CUI: C0027122
Disease: Myositis Ossificans
Myositis Ossificans 		12 0 2 7.7E-02 0 0
CUI: C1112459
Disease: Unresectable Hepatocellular Carcinoma
Unresectable Hepatocellular Carcinoma 		14 0 2 7.1E-02 0 0
CUI: C1853230
Disease: Aphakia, congenital primary
Aphakia, congenital primary 		14 0 2 7.1E-02 0 0
CUI: C2931673
Disease: Ceroid lipofuscinosis, neuronal 1, infantile
Ceroid lipofuscinosis, neuronal 1, infantile 		14 0 2 7.1E-02 0 0
CUI: C3839589
Disease: Secondary osteoporosis
Secondary osteoporosis 		15 0 2 6.9E-02 0 0
CUI: C0264122
Disease: Atrophy, Disuse
Atrophy, Disuse 		16 0 2 6.7E-02 0 0
CUI: C0278506
Disease: Non-small cell lung cancer stage III
Non-small cell lung cancer stage III 		16 0 2 6.7E-02 0 0
CUI: C0679407
Disease: Gastrointestinal dysfunction
Gastrointestinal dysfunction 		16 0 2 6.7E-02 0 0