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: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 3.2E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 2 6.3E-03
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant 		0 7 0 0 1 3.1E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 1 3.2E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 1 3.2E-03
CUI: C1834750
Disease: CORONARY ARTERY DISEASE, MODIFIER OF
CORONARY ARTERY DISEASE, MODIFIER OF 		0 1 0 0 1 3.2E-03
CUI: C1834751
Disease: CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV 		0 1 0 0 1 3.2E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 3.1E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 3.2E-03
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO 		0 1 0 0 1 3.2E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 3.2E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia 		0 3 0 0 2 6.3E-03
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 1 4.6E-04 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic 		46 0 1 4.6E-04 0 0
CUI: C4024926
Disease: Focal T2 hyperintense basal ganglia lesion
Focal T2 hyperintense basal ganglia lesion 		46 0 1 4.6E-04 0 0
CUI: C1849488
Disease: Increased serum pyruvate
Increased serum pyruvate 		45 0 1 4.6E-04 0 0
CUI: C3278975
Disease: Attenuation of retinal blood vessels
Attenuation of retinal blood vessels 		41 0 1 4.6E-04 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		40 0 1 4.6E-04 0 0
CUI: C4021608
Disease: Shortening of all distal phalanges of the fingers
Shortening of all distal phalanges of the fingers 		40 0 1 4.6E-04 0 0
CUI: C1839603
Disease: Proximal tubulopathy
Proximal tubulopathy 		37 0 1 4.7E-04 0 0
CUI: C4025844
Disease: Abnormal chorioretinal morphology
Abnormal chorioretinal morphology 		36 0 1 4.7E-04 0 0
CUI: C1839888
Disease: Decreased activity of the pyruvate dehydrogenase complex
Decreased activity of the pyruvate dehydrogenase complex 		35 0 1 4.7E-04 0 0
CUI: C1846151
Disease: Widened subarachnoid space
Widened subarachnoid space 		35 0 1 4.7E-04 0 0
CUI: C4024609
Disease: Decreased activity of mitochondrial respiratory chain
Decreased activity of mitochondrial respiratory chain 		34 0 1 4.7E-04 0 0
CUI: C4024664
Disease: Moderate sensorineural hearing impairment
Moderate sensorineural hearing impairment 		34 0 1 4.7E-04 0 0