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: C0033923
Disease: Psychomotor Performance
Psychomotor Performance 		0 1 0 0 1 1.5E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 1.5E-03
CUI: C0202252
Disease: VITAMIN B12 MEASUREMENT
VITAMIN B12 MEASUREMENT 		0 22 0 0 1 1.5E-03
CUI: C0262436
Disease: Cardiac valvular dysplasia, X-linked
Cardiac valvular dysplasia, X-linked 		0 4 0 0 1 1.5E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 1.5E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 3.0E-03
CUI: C0342942
Disease: Generalized obesity
Generalized obesity 		0 4 0 0 1 1.5E-03
CUI: C0523631
Disease: Folic acid measurement
Folic acid measurement 		0 8 0 0 1 1.5E-03
CUI: C1290646
Disease: Acute apical abscess
Acute apical abscess 		0 3 0 0 1 1.5E-03
CUI: C1832465
Disease: Atrophia Maculosa Varioliformis Cutis, Familial
Atrophia Maculosa Varioliformis Cutis, Familial 		0 1 0 0 1 1.5E-03
CUI: C1834155
Disease: HYPERTENSION, RESISTANT TO CONVENTIONAL THERAPY
HYPERTENSION, RESISTANT TO CONVENTIONAL THERAPY 		0 1 0 0 1 1.5E-03
CUI: C1834750
Disease: CORONARY ARTERY DISEASE, MODIFIER OF
CORONARY ARTERY DISEASE, MODIFIER OF 		0 1 0 0 1 1.5E-03
CUI: C1834751
Disease: CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV 		0 1 0 0 1 1.5E-03
CUI: C1856058
Disease: HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY
HOMOCYSTINURIA DUE TO DEFICIENCY OF N(5,10)-METHYLENETETRAHYDROFOLATE REDUCTASE ACTIVITY 		0 78 0 0 1 1.4E-03
CUI: C1856061
Disease: Methylenetetrahydrofolate reductase deficiency
Methylenetetrahydrofolate reductase deficiency 		0 4 0 0 1 1.5E-03
CUI: C1862591
Disease: CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO
CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO 		0 1 0 0 1 1.5E-03
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO 		0 1 0 0 1 1.5E-03
CUI: C1853487
Disease: Thick eyebrow
Thick eyebrow 		104 0 1 1.3E-03 0 0
CUI: C0426886
Disease: Tapering fingers (finding)
Tapering fingers (finding) 		91 0 1 1.3E-03 0 0
CUI: C1853738
Disease: Long eyelashes
Long eyelashes 		83 0 1 1.3E-03 0 0
CUI: C2699541
Disease: Cytokine Measurement
Cytokine Measurement 		82 0 1 1.3E-03 0 0
CUI: C1839767
Disease: Tented upper lip vermilion
Tented upper lip vermilion 		79 0 1 1.3E-03 0 0
CUI: C1838391
Disease: Limb hypertonia
Limb hypertonia 		77 0 1 1.3E-03 0 0
CUI: C1445953
Disease: Poor eye contact
Poor eye contact 		73 0 1 1.3E-03 0 0
CUI: C1842581
Disease: Abnormal corpus callosum morphology
Abnormal corpus callosum morphology 		70 0 1 1.3E-03 0 0