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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.2E-03
CUI: C0268958
Disease: Acute orchitis
Acute orchitis 		0 1 0 0 1 1.2E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 1.2E-03
CUI: C0302356
Disease: incomplete anencephaly, hemicrania
incomplete anencephaly, hemicrania 		0 1 0 0 1 1.2E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 2.4E-03
CUI: C0751696
Disease: Post-Traumatic Vegetative State
Post-Traumatic Vegetative State 		0 2 0 0 1 1.2E-03
CUI: C0752197
Disease: Adult-Onset Dystonias
Adult-Onset Dystonias 		0 2 0 0 1 1.2E-03
CUI: C0859021
Disease: Hyperthymic state
Hyperthymic state 		0 5 0 0 1 1.2E-03
CUI: C0865304
Disease: Schizophreniform psychosis NOS
Schizophreniform psychosis NOS 		0 2 0 0 1 1.2E-03
CUI: C1290646
Disease: Acute apical abscess
Acute apical abscess 		0 3 0 0 1 1.2E-03
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy 		0 9 0 0 1 1.2E-03
CUI: C1833450
Disease: HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO 		0 1 0 0 1 1.2E-03
CUI: C1834750
Disease: CORONARY ARTERY DISEASE, MODIFIER OF
CORONARY ARTERY DISEASE, MODIFIER OF 		0 1 0 0 1 1.2E-03
CUI: C1834751
Disease: CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV 		0 1 0 0 1 1.2E-03
CUI: C1840136
Disease: DIABETES MELLITUS, INSULIN-DEPENDENT, SUSCEPTIBILITY TO
DIABETES MELLITUS, INSULIN-DEPENDENT, SUSCEPTIBILITY TO 		0 1 0 0 1 1.2E-03
CUI: C1857845
Disease: CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding) 		0 1 0 0 1 1.2E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 1.2E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.2E-03
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO 		0 1 0 0 1 1.2E-03
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		104 0 1 6.4E-04 0 0
CUI: C1842581
Disease: Abnormal corpus callosum morphology
Abnormal corpus callosum morphology 		70 0 1 6.5E-04 0 0
CUI: C1850456
Disease: Progressive microcephaly
Progressive microcephaly 		67 0 1 6.6E-04 0 0
CUI: C1847514
Disease: Postnatal microcephaly
Postnatal microcephaly 		62 0 1 6.6E-04 0 0
CUI: C0235095
Disease: Visual field constriction
Visual field constriction 		57 0 1 6.6E-04 0 0
CUI: C0266642
Disease: Situs ambiguus
Situs ambiguus 		55 0 1 6.6E-04 0 0