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: C0391970
Disease: Carcinoid tumor, malignant
Carcinoid tumor, malignant 		0 2 0 0 2 2.9E-03
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 1.4E-03
CUI: C0432562
Disease: Malignant lymphoma of spleen
Malignant lymphoma of spleen 		0 2 0 0 2 2.9E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 1.4E-03
CUI: C0028077
Disease: Nyctalopia
Nyctalopia 		168 0 1 1.8E-03 0 0
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		163 0 1 1.8E-03 0 0
CUI: C0431447
Disease: Synophrys
Synophrys 		111 0 1 2.0E-03 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect 		94 0 1 2.1E-03 0 0
CUI: C0337438
Disease: Glucose measurement
Glucose measurement 		89 0 1 2.1E-03 0 0
CUI: C0495706
Disease: elevated blood glucose level
elevated blood glucose level 		89 0 1 2.1E-03 0 0
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate 		87 0 1 2.1E-03 0 0
CUI: C4021611
Disease: Abnormality of epiphysis morphology
Abnormality of epiphysis morphology 		86 0 1 2.1E-03 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		85 0 1 2.1E-03 0 0
CUI: C1857108
Disease: Limitation of joint mobility
Limitation of joint mobility 		84 0 1 2.1E-03 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea 		82 0 1 2.2E-03 0 0
CUI: C0600031
Disease: Congenital absence of spleen
Congenital absence of spleen 		80 0 1 2.2E-03 0 0
CUI: C1834055
Disease: Underdeveloped nasal alae
Underdeveloped nasal alae 		79 0 1 2.2E-03 0 0
CUI: C1527366
Disease: Salaam Seizures
Salaam Seizures 		75 0 1 2.2E-03 0 0
CUI: C3554617
Disease: Adducted thumb
Adducted thumb 		74 0 1 2.2E-03 0 0
CUI: C0409338
Disease: Flexion contracture - elbow
Flexion contracture - elbow 		73 0 1 2.2E-03 0 0
CUI: C1445953
Disease: Poor eye contact
Poor eye contact 		73 0 1 2.2E-03 0 0
CUI: C0542514
Disease: Blue sclera
Blue sclera 		70 0 1 2.2E-03 0 0
CUI: C1842581
Disease: Abnormal corpus callosum morphology
Abnormal corpus callosum morphology 		70 0 1 2.2E-03 0 0
CUI: C0085682
Disease: Hypophosphatemia
Hypophosphatemia 		69 0 1 2.2E-03 0 0
CUI: C0271097
Disease: Usher Syndrome
Usher Syndrome 		68 0 1 2.2E-03 0 0