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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 2.3E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 2.4E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 2.3E-03
CUI: C0268958
Disease: Acute orchitis
Acute orchitis 		0 1 0 0 1 2.4E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 2.4E-03
CUI: C0302356
Disease: incomplete anencephaly, hemicrania
incomplete anencephaly, hemicrania 		0 1 0 0 1 2.4E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 4.7E-03
CUI: C0751771
Disease: Sleep Bruxism
Sleep Bruxism 		0 4 0 0 1 2.3E-03
CUI: C1281440
Disease: Familial obesity
Familial obesity 		0 3 0 0 1 2.3E-03
CUI: C1290646
Disease: Acute apical abscess
Acute apical abscess 		0 3 0 0 2 4.7E-03
CUI: C1833450
Disease: HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO 		0 1 0 0 1 2.4E-03
CUI: C1834750
Disease: CORONARY ARTERY DISEASE, MODIFIER OF
CORONARY ARTERY DISEASE, MODIFIER OF 		0 1 0 0 1 2.4E-03
CUI: C1834751
Disease: CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV 		0 1 0 0 1 2.4E-03
CUI: C1857845
Disease: CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding) 		0 1 0 0 1 2.4E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 2.4E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 2.3E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.4E-03
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO 		0 1 0 0 1 2.4E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 4.7E-03
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 1 1.1E-03 0 0
CUI: C0339526
Disease: Autosomal recessive retinitis pigmentosa
Autosomal recessive retinitis pigmentosa 		82 0 1 1.1E-03 0 0
CUI: C0241726
Disease: Delayed ability to walk
Delayed ability to walk 		77 0 1 1.1E-03 0 0
CUI: C1850456
Disease: Progressive microcephaly
Progressive microcephaly 		67 0 1 1.1E-03 0 0
CUI: C3501844
Disease: Familial Nonmedullary Thyroid Cancer
Familial Nonmedullary Thyroid Cancer 		66 0 1 1.1E-03 0 0
CUI: C1847514
Disease: Postnatal microcephaly
Postnatal microcephaly 		62 0 1 1.1E-03 0 0