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 9.7E-03
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 9.7E-03
CUI: C0518964
Disease: BRONCHIAL ADENOCARCINOMA
BRONCHIAL ADENOCARCINOMA
0 1 0 0 1 9.7E-03
CUI: C0523979
Disease: Vitamin D3 measurement
Vitamin D3 measurement
0 51 0 0 2 1.3E-02
Severe nonproliferative diabetic retinopathy
0 3 0 0 1 9.5E-03
CUI: C0741585
Disease: BODY ACHE
BODY ACHE
0 1 0 0 1 9.7E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort
0 2 0 0 2 1.9E-02
CUI: C0919758
Disease: Vitamin D measurement
Vitamin D measurement
0 51 0 0 2 1.3E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 9.7E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 9.7E-03
CUI: C3890602
Disease: Bodily Pain
Bodily Pain
0 4 0 0 1 9.4E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 1 9.5E-03
CUI: C1167918
Disease: Increased CSF lactate
Increased CSF lactate
87 0 1 9.7E-04 0 0
CUI: C1838391
Disease: Limb hypertonia
Limb hypertonia
77 0 1 9.8E-04 0 0
CUI: C1847514
Disease: Postnatal microcephaly
Postnatal microcephaly
62 0 1 9.9E-04 0 0
CUI: C1855483
Disease: Progressive spastic paraplegia
Progressive spastic paraplegia
59 0 1 9.9E-04 0 0
CUI: C0202177
Disease: Phospholipid measurement
Phospholipid measurement
58 0 1 9.9E-04 0 0
CUI: C0040485
Disease: Torticollis
Torticollis
55 0 1 1.0E-03 0 0
CUI: C0337428
Disease: Fibrinogen assay
Fibrinogen assay
55 0 1 1.0E-03 0 0
CUI: C1842688
Disease: Hypoplasia of the brainstem
Hypoplasia of the brainstem
55 0 1 1.0E-03 0 0
CUI: C0234182
Disease: Gowers sign
Gowers sign
54 0 1 1.0E-03 0 0
Serum gamma-glutamyl transferase measurement
54 0 1 1.0E-03 0 0
CUI: C1306620
Disease: Systolic blood pressure measurement
Systolic blood pressure measurement
54 0 1 1.0E-03 0 0
CUI: C4021219
Disease: Multifocal epileptiform discharges
Multifocal epileptiform discharges
52 0 1 1.0E-03 0 0
CUI: C0027877
Disease: Neuronal Ceroid-Lipofuscinoses
Neuronal Ceroid-Lipofuscinoses
51 0 1 1.0E-03 0 0