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: C0206368
Disease: Exfoliation Syndrome
Exfoliation Syndrome 		0 74 0 0 1 9.0E-04
CUI: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement 		0 51 0 0 2 1.8E-03
CUI: C0919758
Disease: Vitamin D measurement
Vitamin D measurement 		0 51 0 0 2 1.8E-03
CUI: C4280669
Disease: Velopharyngeal dysfunction
Velopharyngeal dysfunction 		0 33 0 0 1 9.4E-04
CUI: C0015230
Disease: Exanthema
Exanthema 		251 0 1 1.5E-03 0 0
CUI: C0563625
Disease: Agnosia for Pain
Agnosia for Pain 		204 0 1 1.7E-03 0 0
CUI: C0271623
Disease: Hypogonadotropic hypogonadism
Hypogonadotropic hypogonadism 		178 0 1 1.7E-03 0 0
CUI: C4290046
Disease: trachomatis
trachomatis 		175 0 1 1.7E-03 0 0
CUI: C0338831
Disease: Manic
Manic 		166 0 1 1.8E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression 		165 0 1 1.8E-03 0 0
CUI: C0030499
Disease: Parasitic Diseases
Parasitic Diseases 		164 0 1 1.8E-03 0 0
CUI: C0024419
Disease: Waldenstrom Macroglobulinemia
Waldenstrom Macroglobulinemia 		162 0 1 1.8E-03 0 0
CUI: C0022735
Disease: Klinefelter Syndrome
Klinefelter Syndrome 		150 0 1 1.8E-03 0 0
CUI: C0024266
Disease: Lymphocytic Choriomeningitis
Lymphocytic Choriomeningitis 		147 0 1 1.8E-03 0 0
CUI: C0338908
Disease: Mixed anxiety and depressive disorder
Mixed anxiety and depressive disorder 		146 0 1 1.8E-03 0 0
CUI: C1858430
Disease: Death in infancy
Death in infancy 		146 0 1 1.8E-03 0 0
CUI: C0009171
Disease: Cocaine Abuse
Cocaine Abuse 		144 0 1 1.8E-03 0 0
CUI: C0037772
Disease: Spastic Paraplegia
Spastic Paraplegia 		144 0 1 1.8E-03 0 0
CUI: C0014173
Disease: Endometrial Hyperplasia
Endometrial Hyperplasia 		143 0 1 1.8E-03 0 0
CUI: C0151825
Disease: Bone pain
Bone pain 		139 0 1 1.9E-03 0 0
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		137 0 1 1.9E-03 0 0
CUI: C0020097
Disease: HTLV-I Infections
HTLV-I Infections 		134 0 1 1.9E-03 0 0
CUI: C0013473
Disease: Eating Disorders
Eating Disorders 		133 0 1 1.9E-03 0 0
CUI: C0043119
Disease: Werner Syndrome
Werner Syndrome 		130 0 1 1.9E-03 0 0
CUI: C0232939
Disease: Primary physiologic amenorrhea
Primary physiologic amenorrhea 		129 0 1 1.9E-03 0 0