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 4.5E-03
CUI: C0342759
Disease: Primary lactose intolerance
Primary lactose intolerance 		0 1 0 0 1 4.5E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort 		0 2 0 0 2 9.0E-03
CUI: C1862591
Disease: CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO
CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO 		0 1 0 0 1 4.5E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia 		0 1 0 0 1 4.5E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 4.5E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 4.5E-03
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 1 4.2E-04 0 0
CUI: C0018810
Disease: heart rate
heart rate 		36 0 1 4.2E-04 0 0
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		33 9 1 4.2E-04 1 4.3E-03
CUI: C1845251
Disease: Facial hypotonia
Facial hypotonia 		33 0 1 4.2E-04 0 0
CUI: C3806218
Disease: Episodic tachypnea
Episodic tachypnea 		31 0 1 4.2E-04 0 0
CUI: C1855676
Disease: Aplasia/Hypoplasia of the cerebellar vermis
Aplasia/Hypoplasia of the cerebellar vermis 		30 0 1 4.2E-04 0 0
CUI: C0265275
Disease: Jeune thoracic dystrophy
Jeune thoracic dystrophy 		29 0 1 4.2E-04 0 0
CUI: C1321329
Disease: Slowed saccades
Slowed saccades 		29 0 1 4.2E-04 0 0
CUI: C2677328
Disease: Cerebral hypomyelination
Cerebral hypomyelination 		29 0 1 4.2E-04 0 0
CUI: C3715208
Disease: AV Block First Degree by ECG Finding
AV Block First Degree by ECG Finding 		28 0 1 4.2E-04 0 0
CUI: C1720824
Disease: Sudden Cardiac Arrest
Sudden Cardiac Arrest 		27 0 1 4.2E-04 0 0
CUI: C0265215
Disease: Meckel-Gruber syndrome
Meckel-Gruber syndrome 		26 0 1 4.2E-04 0 0
CUI: C0728895
Disease: Absent finger
Absent finger 		26 0 1 4.2E-04 0 0
CUI: C0238111
Disease: Lennox-Gastaut syndrome
Lennox-Gastaut syndrome 		25 0 1 4.2E-04 0 0
CUI: C0333751
Disease: Muscle fiber atrophy
Muscle fiber atrophy 		25 0 1 4.2E-04 0 0
CUI: C0030591
Disease: Paroxysmal ventricular tachycardia
Paroxysmal ventricular tachycardia 		24 0 1 4.2E-04 0 0
CUI: C4021728
Disease: EMG: decremental response of compound muscle action potential to repetitive nerve stimulation
EMG: decremental response of compound muscle action potential to repetitive nerve stimulation 		24 0 1 4.2E-04 0 0
CUI: C0155707
Disease: Trifascicular block
Trifascicular block 		23 0 1 4.2E-04 0 0