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 3.3E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 3.4E-03
CUI: C0162296
Disease: Polyarthralgia
Polyarthralgia 		0 1 0 0 1 3.4E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 3.3E-03
CUI: C0393761
Disease: Middle insomnia
Middle insomnia 		0 1 0 0 1 3.4E-03
CUI: C1401162
Disease: Carbohydrate intolerance
Carbohydrate intolerance 		0 1 0 0 1 3.4E-03
CUI: C1843898
Disease: BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 (disorder)
BODY MASS INDEX QUANTITATIVE TRAIT LOCUS 4 (disorder) 		0 1 0 0 1 3.4E-03
CUI: C1852324
Disease: ALDOSTERONE TO RENIN RATIO, INCREASED
ALDOSTERONE TO RENIN RATIO, INCREASED 		0 1 0 0 1 3.4E-03
CUI: C1864275
Disease: SCHIZOPHRENIA 6 (disorder)
SCHIZOPHRENIA 6 (disorder) 		0 1 0 0 1 3.4E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 3.4E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 3.4E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 3.4E-03
CUI: C3888516
Disease: CYP1A2 polymorphism
CYP1A2 polymorphism 		0 2 0 0 1 3.4E-03
CUI: C4016708
Disease: HYPERTENSION, EARLY-ONSET, AUTOSOMAL DOMINANT, WITH EXACERBATION IN PREGNANCY
HYPERTENSION, EARLY-ONSET, AUTOSOMAL DOMINANT, WITH EXACERBATION IN PREGNANCY 		0 1 0 0 1 3.4E-03
CUI: C4022560
Disease: Splanchnic vein thrombosis
Splanchnic vein thrombosis 		0 2 0 0 1 3.4E-03
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia 		0 9 0 0 1 3.3E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 6.8E-03
CUI: C0152421
Disease: Macrotia
Macrotia 		188 0 1 1.6E-03 0 0
CUI: C0240063
Disease: Coloboma of iris
Coloboma of iris 		153 0 1 1.7E-03 0 0
CUI: C0266551
Disease: Congenital coloboma of iris
Congenital coloboma of iris 		148 0 1 1.7E-03 0 0
CUI: C1136249
Disease: Mental Retardation, X-Linked
Mental Retardation, X-Linked 		141 0 1 1.7E-03 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria 		129 0 1 1.7E-03 0 0
CUI: C0030232
Disease: Pallor
Pallor 		124 0 1 1.8E-03 0 0
CUI: C0427065
Disease: Distal muscle weakness
Distal muscle weakness 		117 0 1 1.8E-03 0 0
CUI: C0452138
Disease: Sensorineural hearing loss, bilateral
Sensorineural hearing loss, bilateral 		117 0 1 1.8E-03 0 0