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 6.6E-03
CUI: C0085666
Disease: Spider nevus
Spider nevus
0 2 0 0 1 6.6E-03
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
0 1 0 0 1 6.6E-03
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
0 1 0 0 1 6.6E-03
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 6.6E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 6.6E-03
CUI: C0231835
Disease: Tachypnea
Tachypnea
82 0 1 4.3E-04 0 0
CUI: C0022521
Disease: Kartagener Syndrome
Kartagener Syndrome
67 0 1 4.3E-04 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
59 0 1 4.3E-04 0 0
CUI: C0018520
Disease: Halitosis
Halitosis
48 0 1 4.4E-04 0 0
CUI: C0376532
Disease: Epilepsy, Rolandic
Epilepsy, Rolandic
46 0 1 4.4E-04 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance
44 0 1 4.4E-04 0 0
Thyroid stimulating hormone measurement
42 0 1 4.4E-04 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination
40 0 1 4.4E-04 0 0
LEIGH SYNDROME DUE TO MITOCHONDRIAL COMPLEX I DEFICIENCY
40 0 1 4.4E-04 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome
39 0 1 4.4E-04 0 0
CUI: C1839603
Disease: Proximal tubulopathy
Proximal tubulopathy
37 0 1 4.4E-04 0 0
Leigh Syndrome due to Mitochondrial Complex IV Deficiency
37 0 1 4.4E-04 0 0
Leigh Syndrome Due To Mitochondrial Complex II Deficiency
36 0 1 4.4E-04 0 0
Leigh Syndrome due to Mitochondrial Complex III Deficiency
36 0 1 4.4E-04 0 0
Leigh Syndrome due to Mitochondrial Complex V Deficiency
36 0 1 4.4E-04 0 0
Necrotizing encephalopathy, infantile subacute, of Leigh
36 0 1 4.4E-04 0 0
Diastolic blood pressure measurement
35 0 1 4.4E-04 0 0
Focal T2 hyperintense brainstem lesion
33 0 1 4.4E-04 0 0
CUI: C0151818
Disease: Opisthotonus
Opisthotonus
32 0 1 4.4E-04 0 0