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 5.2E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 5.4E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 5.3E-03
CUI: C0393761
Disease: Middle insomnia
Middle insomnia 		0 1 0 0 1 5.4E-03
CUI: C1406659
Disease: Symptomatic epilepsy
Symptomatic epilepsy 		0 9 0 0 1 5.2E-03
CUI: C1832615
Disease: HYPERPARATHYROIDISM, NEONATAL SEVERE
HYPERPARATHYROIDISM, NEONATAL SEVERE 		0 14 0 0 1 5.1E-03
CUI: C1837217
Disease: Cleft lip, isolated
Cleft lip, isolated 		0 2 0 0 1 5.4E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 5.4E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 5.4E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 5.4E-03
CUI: C4694057
Disease: Taq1A POLYMORPHISM
Taq1A POLYMORPHISM 		0 14 0 0 2 1.0E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 1.1E-02
CUI: C1861324
Disease: Short philtrum
Short philtrum 		182 0 1 1.5E-03 0 0
CUI: C1868571
Disease: Highly arched eyebrow
Highly arched eyebrow 		141 0 1 1.6E-03 0 0
CUI: C0152423
Disease: Congenital small ears
Congenital small ears 		137 0 1 1.6E-03 0 0
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment 		136 0 1 1.7E-03 0 0
CUI: C0014877
Disease: Esotropia
Esotropia 		121 0 1 1.7E-03 0 0
CUI: C1842876
Disease: Depressed nasal ridge
Depressed nasal ridge 		117 0 1 1.7E-03 0 0
CUI: C1277241
Disease: Delayed myelination
Delayed myelination 		112 0 1 1.7E-03 0 0
CUI: C1861866
Disease: Aplasia/Hypoplasia of the corpus callosum
Aplasia/Hypoplasia of the corpus callosum 		108 0 1 1.7E-03 0 0
CUI: C1839758
Disease: Narrow forehead
Narrow forehead 		106 0 1 1.7E-03 0 0
CUI: C1840379
Disease: Cerebellar vermis hypoplasia
Cerebellar vermis hypoplasia 		100 0 1 1.8E-03 0 0
CUI: C0578038
Disease: Thin lips
Thin lips 		99 0 1 1.8E-03 0 0
CUI: C0424230
Disease: Motor retardation
Motor retardation 		98 0 1 1.8E-03 0 0
CUI: C0013132
Disease: Drooling
Drooling 		95 0 1 1.8E-03 0 0