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 3.5E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus
0 2 0 0 2 7.1E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 2 7.1E-03
Severe nonproliferative diabetic retinopathy
0 3 0 0 2 7.0E-03
CUI: C0745031
Disease: homicidal
homicidal
0 2 0 0 1 3.5E-03
CUI: C1318233
Disease: immunoglobulin G index
immunoglobulin G index
0 4 0 0 1 3.5E-03
CUI: C1446147
Disease: IgG Index (procedure)
IgG Index (procedure)
0 4 0 0 1 3.5E-03
ALZHEIMER DISEASE, SUSCEPTIBILITY TO
0 3 0 0 1 3.5E-03
CUI: C2674950
Disease: LUNG CANCER, SUSCEPTIBILITY TO
LUNG CANCER, SUSCEPTIBILITY TO
0 3 0 0 2 7.0E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 3.5E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 3.5E-03
VASCULAR DEMENTIA, SUSCEPTIBILITY TO
0 1 0 0 1 3.5E-03
Frequent episodic tension-type headache
0 1 0 0 1 3.5E-03
CUI: C0231835
Disease: Tachypnea
Tachypnea
82 0 1 5.1E-04 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
59 0 1 5.2E-04 0 0
CUI: C0234182
Disease: Gowers sign
Gowers sign
54 0 1 5.2E-04 0 0
CUI: C0018520
Disease: Halitosis
Halitosis
48 0 1 5.2E-04 0 0
CUI: C0271385
Disease: Horizontal Nystagmus
Horizontal Nystagmus
48 0 1 5.2E-04 0 0
CUI: C0730290
Disease: Cone Dystrophy
Cone Dystrophy
48 0 1 5.2E-04 0 0
CUI: C1855925
Disease: Hyperopia, High
Hyperopia, High
47 0 1 5.2E-04 0 0
Thyroid stimulating hormone measurement
42 0 1 5.2E-04 0 0
CUI: C0234860
Disease: Weak cry
Weak cry
42 0 1 5.2E-04 0 0
CUI: C0429097
Disease: QRS complex feature
QRS complex feature
41 0 1 5.2E-04 0 0
Decreased activity of mitochondrial complex I
41 0 1 5.2E-04 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination
40 0 1 5.2E-04 0 0