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 4.1E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus 		0 2 0 0 2 8.2E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis 		0 2 0 0 2 8.2E-03
CUI: C0730278
Disease: Severe nonproliferative diabetic retinopathy
Severe nonproliferative diabetic retinopathy 		0 3 0 0 2 8.1E-03
CUI: C0745031
Disease: homicidal
homicidal 		0 2 0 0 1 4.1E-03
CUI: C1856170
Disease: ALZHEIMER DISEASE, SUSCEPTIBILITY TO
ALZHEIMER DISEASE, SUSCEPTIBILITY TO 		0 3 0 0 1 4.0E-03
CUI: C2674950
Disease: LUNG CANCER, SUSCEPTIBILITY TO
LUNG CANCER, SUSCEPTIBILITY TO 		0 3 0 0 2 8.1E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal 		0 3 0 0 1 4.0E-03
CUI: C3875381
Disease: Homozygous methylenetetrahydrofolate reductase mutation
Homozygous methylenetetrahydrofolate reductase mutation 		0 1 0 0 1 4.1E-03
CUI: C4016417
Disease: VASCULAR DEMENTIA, SUSCEPTIBILITY TO
VASCULAR DEMENTIA, SUSCEPTIBILITY TO 		0 1 0 0 1 4.1E-03
CUI: C4302174
Disease: Frequent episodic tension-type headache
Frequent episodic tension-type headache 		0 1 0 0 1 4.1E-03
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		59 0 1 5.6E-04 0 0
CUI: C0234182
Disease: Gowers sign
Gowers sign 		54 0 1 5.6E-04 0 0
CUI: C0018520
Disease: Halitosis
Halitosis 		48 0 1 5.7E-04 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus 		48 0 1 5.7E-04 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy 		48 0 1 5.7E-04 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High 		47 0 1 5.7E-04 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance 		44 0 1 5.7E-04 0 0
CUI: C0202230
Disease: Thyroid stimulating hormone measurement
Thyroid stimulating hormone measurement 		42 0 1 5.7E-04 0 0
CUI: C0234860
Disease: Weak cry
Weak cry 		42 0 1 5.7E-04 0 0
CUI: C2677650
Disease: Decreased activity of mitochondrial complex I
Decreased activity of mitochondrial complex I 		41 0 1 5.7E-04 0 0
CUI: C0085606
Disease: Urgency of micturition
Urgency of micturition 		40 0 1 5.7E-04 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination 		40 0 1 5.7E-04 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome 		39 0 1 5.7E-04 0 0
CUI: C0151878
Disease: Prolonged QT interval
Prolonged QT interval 		38 0 1 5.7E-04 0 0