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: C0005750
Disease: Blind Loop Syndrome
Blind Loop Syndrome 		0 3 0 0 1 1.0E-01
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 6.2E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 0.12
CUI: C0036337
Disease: Schizoaffective Disorder
Schizoaffective Disorder 		0 61 0 0 1 1.5E-02
CUI: C0043346
Disease: Xeroderma Pigmentosum
Xeroderma Pigmentosum 		0 35 0 0 1 2.4E-02
CUI: C0085119
Disease: Foot Ulcer
Foot Ulcer 		0 3 0 0 1 1.0E-01
CUI: C0206172
Disease: Diabetic Foot
Diabetic Foot 		0 13 0 0 1 5.0E-02
CUI: C0242453
Disease: Prostatism
Prostatism 		0 1 0 0 1 0.12
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 7.1E-02
CUI: C0272275
Disease: Heparin-induced thrombocytopenia with thrombosis
Heparin-induced thrombocytopenia with thrombosis 		0 1 0 0 1 0.12
CUI: C0339510
Disease: Vitelliform Macular Dystrophy
Vitelliform Macular Dystrophy 		0 120 0 0 2 1.6E-02
CUI: C0342342
Disease: Idiopathic Hypoparathyroidism
Idiopathic Hypoparathyroidism 		0 5 0 0 1 8.3E-02
CUI: C0375071
Disease: Malignant neoplasm of vulva
Malignant neoplasm of vulva 		0 2 0 0 1 0.11
CUI: C0677055
Disease: CARCINOMA OF VULVA
CARCINOMA OF VULVA 		0 2 0 0 1 0.11
CUI: C0948698
Disease: Coronary spastic angina
Coronary spastic angina 		0 1 0 0 1 0.12
CUI: C1321551
Disease: Shprintzen-Goldberg syndrome
Shprintzen-Goldberg syndrome 		0 21 0 0 1 3.6E-02
CUI: C1333763
Disease: Gastric Cardia Carcinoma
Gastric Cardia Carcinoma 		0 13 0 0 1 5.0E-02
CUI: C1834155
Disease: HYPERTENSION, RESISTANT TO CONVENTIONAL THERAPY
HYPERTENSION, RESISTANT TO CONVENTIONAL THERAPY 		0 1 0 0 1 0.12
CUI: C1837217
Disease: Cleft lip, isolated
Cleft lip, isolated 		0 2 0 0 1 0.11
CUI: C3164407
Disease: Oligoasthenozoospermia
Oligoasthenozoospermia 		0 6 0 0 1 7.7E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 0.12
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 0.12
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 1 1.0E-01
CUI: C0410702
Disease: Adolescent idiopathic scoliosis
Adolescent idiopathic scoliosis 		656 0 1 1.4E-03 0 0
CUI: C0021704
Disease: Intelligence
Intelligence 		645 0 1 1.5E-03 0 0