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 2.9E-03
CUI: C0272292
Disease: Acute idiopathic thrombocytopenic purpura
Acute idiopathic thrombocytopenic purpura 		0 1 0 0 1 2.9E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 5.9E-03
CUI: C0423461
Disease: Cilioretinal artery (disorder)
Cilioretinal artery (disorder) 		0 1 0 0 1 2.9E-03
CUI: C0476482
Disease: Restlessness and agitation
Restlessness and agitation 		0 1 0 0 1 2.9E-03
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 2.9E-03
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse 		0 1 0 0 1 2.9E-03
CUI: C1834750
Disease: CORONARY ARTERY DISEASE, MODIFIER OF
CORONARY ARTERY DISEASE, MODIFIER OF 		0 1 0 0 1 2.9E-03
CUI: C1834751
Disease: CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV 		0 1 0 0 1 2.9E-03
CUI: C1843807
Disease: Basal ganglia disease, biotin-responsive
Basal ganglia disease, biotin-responsive 		0 19 0 0 1 2.8E-03
CUI: C1969810
Disease: FEBRILE CONVULSIONS, FAMILIAL, 8
FEBRILE CONVULSIONS, FAMILIAL, 8 		0 13 0 0 1 2.8E-03
CUI: C3178803
Disease: Social Anhedonia
Social Anhedonia 		0 4 0 0 1 2.9E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 2.9E-03
CUI: C3825385
Disease: Epilepsy in adolescence
Epilepsy in adolescence 		0 1 0 0 1 2.9E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 2.9E-03
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO 		0 1 0 0 1 2.9E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 2.9E-03
CUI: C4693613
Disease: EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 10
EPILEPSY, JUVENILE MYOCLONIC, SUSCEPTIBILITY TO, 10 		0 5 0 0 1 2.9E-03
CUI: C4024818
Disease: Progressive night blindness
Progressive night blindness 		87 0 1 7.7E-04 0 0
CUI: C0231835
Disease: Tachypnea
Tachypnea 		82 0 1 7.7E-04 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome 		67 0 1 7.8E-04 0 0
CUI: C0919677
Disease: Protein C measurement
Protein C measurement 		62 0 1 7.8E-04 0 0
CUI: C1168438
Disease: Protein C antigen measurement
Protein C antigen measurement 		62 0 1 7.8E-04 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 0 1 7.9E-04 0 0
CUI: C4551906
Disease: Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus 		43 0 1 8.0E-04 0 0