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: C0013504
Disease: Echinococcosis, Hepatic
Echinococcosis, Hepatic 		0 1 0 0 1 1.6E-03
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 1.6E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 1.6E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 1.6E-03
CUI: C0268140
Disease: Xeroderma pigmentosum, group F
Xeroderma pigmentosum, group F 		0 31 0 0 1 1.6E-03
CUI: C0268958
Disease: Acute orchitis
Acute orchitis 		0 1 0 0 1 1.6E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 1.6E-03
CUI: C0302356
Disease: incomplete anencephaly, hemicrania
incomplete anencephaly, hemicrania 		0 1 0 0 1 1.6E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 3.3E-03
CUI: C0947912
Disease: Myasthenias
Myasthenias 		0 3 0 0 2 3.3E-03
CUI: C1334633
Disease: Mature B-Cell Neoplasm
Mature B-Cell Neoplasm 		0 15 0 0 1 1.6E-03
CUI: C1833450
Disease: HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO 		0 1 0 0 1 1.6E-03
CUI: C1840136
Disease: DIABETES MELLITUS, INSULIN-DEPENDENT, SUSCEPTIBILITY TO
DIABETES MELLITUS, INSULIN-DEPENDENT, SUSCEPTIBILITY TO 		0 1 0 0 1 1.6E-03
CUI: C1857845
Disease: CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding) 		0 1 0 0 1 1.6E-03
CUI: C2585575
Disease: Recurrent abdominal pain
Recurrent abdominal pain 		0 2 0 0 1 1.6E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 1.6E-03
CUI: C1866195
Disease: Downturned corners of mouth
Downturned corners of mouth 		122 0 1 1.2E-03 0 0
CUI: C1842876
Disease: Depressed nasal ridge
Depressed nasal ridge 		117 0 1 1.2E-03 0 0
CUI: C1861866
Disease: Aplasia/Hypoplasia of the corpus callosum
Aplasia/Hypoplasia of the corpus callosum 		108 0 1 1.2E-03 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology 		104 0 1 1.2E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis 		104 0 1 1.2E-03 0 0
CUI: C1837142
Disease: Poor suck
Poor suck 		103 0 1 1.2E-03 0 0
CUI: C0240379
Disease: Open mouth (finding)
Open mouth (finding) 		96 0 1 1.2E-03 0 0
CUI: C0431399
Disease: Familial aplasia of the vermis
Familial aplasia of the vermis 		95 0 1 1.2E-03 0 0
CUI: C1720983
Disease: Channelopathies
Channelopathies 		94 0 1 1.2E-03 0 0