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: C0013504
Disease: Echinococcosis, Hepatic
Echinococcosis, Hepatic 		0 1 0 0 1 9.8E-04
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		0 9 0 0 1 9.7E-04
CUI: C0035085
Disease: Renal infarction
Renal infarction 		0 1 0 0 1 9.8E-04
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 1 9.8E-04
CUI: C0268958
Disease: Acute orchitis
Acute orchitis 		0 1 0 0 1 9.8E-04
CUI: C0302356
Disease: incomplete anencephaly, hemicrania
incomplete anencephaly, hemicrania 		0 1 0 0 1 9.8E-04
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 2.0E-03
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 9.8E-04
CUI: C1456332
Disease: Stimulant abuse
Stimulant abuse 		0 1 0 0 1 9.8E-04
CUI: C1833450
Disease: HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO 		0 1 0 0 1 9.8E-04
CUI: C1834750
Disease: CORONARY ARTERY DISEASE, MODIFIER OF
CORONARY ARTERY DISEASE, MODIFIER OF 		0 1 0 0 1 9.8E-04
CUI: C1834751
Disease: CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV
CORONARY ARTERY DISEASE, DEVELOPMENT OF, IN HIV 		0 1 0 0 1 9.8E-04
CUI: C1857845
Disease: CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding) 		0 1 0 0 1 9.8E-04
CUI: C2677565
Disease: AMYOTROPHIC LATERAL SCLEROSIS 10 (disorder)
AMYOTROPHIC LATERAL SCLEROSIS 10 (disorder) 		0 25 0 0 1 9.6E-04
CUI: C3148872
Disease: FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED
FRONTOTEMPORAL DEMENTIA WITH TDP43 INCLUSIONS, TARDBP-RELATED 		0 3 0 0 1 9.8E-04
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 2 2.0E-03
CUI: C3641106
Disease: Congenital Bleeding Disorder
Congenital Bleeding Disorder 		0 2 0 0 1 9.8E-04
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 9.8E-04
CUI: C4016263
Disease: SPINA BIFIDA, SUSCEPTIBILITY TO
SPINA BIFIDA, SUSCEPTIBILITY TO 		0 1 0 0 1 9.8E-04
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 9.8E-04
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 1 5.4E-04 0 0
CUI: C0344530
Disease: Congenital keratoglobus
Congenital keratoglobus 		46 0 1 5.4E-04 0 0
CUI: C0332615
Disease: Myopathic facies
Myopathic facies 		44 0 1 5.4E-04 0 0
CUI: C1855672
Disease: Immotile cilia
Immotile cilia 		41 0 1 5.4E-04 0 0
CUI: C4703436
Disease: Impaired nasal mucociliary clearance
Impaired nasal mucociliary clearance 		41 0 1 5.4E-04 0 0