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: C0001361
Disease: Acute tonsillitis
Acute tonsillitis 		0 1 0 0 1 7.7E-03
CUI: C0242453
Disease: Prostatism
Prostatism 		0 1 0 0 1 7.7E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 7.4E-03
CUI: C0268958
Disease: Acute orchitis
Acute orchitis 		0 1 0 0 1 7.7E-03
CUI: C0278837
Disease: Stage IV Prostate Carcinoma
Stage IV Prostate Carcinoma 		0 6 0 0 1 7.4E-03
CUI: C0302356
Disease: incomplete anencephaly, hemicrania
incomplete anencephaly, hemicrania 		0 1 0 0 1 7.7E-03
CUI: C1837217
Disease: Cleft lip, isolated
Cleft lip, isolated 		0 2 0 0 1 7.6E-03
CUI: C2585575
Disease: Recurrent abdominal pain
Recurrent abdominal pain 		0 2 0 0 1 7.6E-03
CUI: C3146264
Disease: Stage IV Prostate Cancer AJCC v7
Stage IV Prostate Cancer AJCC v7 		0 6 0 0 1 7.4E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 7.6E-03
CUI: C4553752
Disease: Stage IV Prostate Cancer AJCC v8
Stage IV Prostate Cancer AJCC v8 		0 6 0 0 1 7.4E-03
CUI: C0266470
Disease: Cerebellar Hypoplasia
Cerebellar Hypoplasia 		226 0 1 1.5E-03 0 0
CUI: C0423109
Disease: Upward slant of palpebral fissure
Upward slant of palpebral fissure 		216 0 1 1.5E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate 		169 0 1 1.6E-03 0 0
CUI: C1855285
Disease: Protruding ear
Protruding ear 		152 0 1 1.6E-03 0 0
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria 		127 0 1 1.7E-03 0 0
CUI: C0030232
Disease: Pallor
Pallor 		124 0 1 1.7E-03 0 0
CUI: C0014877
Disease: Esotropia
Esotropia 		121 0 1 1.7E-03 0 0
CUI: C1866934
Disease: Reduced tendon reflexes
Reduced tendon reflexes 		121 0 1 1.7E-03 0 0
CUI: C0162701
Disease: Polysomnography
Polysomnography 		119 0 1 1.7E-03 0 0
CUI: C0431447
Disease: Synophrys
Synophrys 		111 23 1 1.8E-03 1 6.6E-03
CUI: C1835884
Disease: Triangular face
Triangular face 		111 0 1 1.8E-03 0 0
CUI: C1609433
Disease: Congenital absence of kidneys syndrome
Congenital absence of kidneys syndrome 		110 0 1 1.8E-03 0 0
CUI: C0240340
Disease: Microdontia (disorder)
Microdontia (disorder) 		109 0 1 1.8E-03 0 0
CUI: C1861866
Disease: Aplasia/Hypoplasia of the corpus callosum
Aplasia/Hypoplasia of the corpus callosum 		108 0 1 1.8E-03 0 0