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 1.0E-03
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 1.0E-03
CUI: C0339805
Disease: Cat allergy (disorder)
Cat allergy (disorder)
0 1 0 0 1 1.0E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 2 2.1E-03
CUI: C1318233
Disease: immunoglobulin G index
immunoglobulin G index
0 4 0 0 1 1.0E-03
CUI: C1446147
Disease: IgG Index (procedure)
IgG Index (procedure)
0 4 0 0 1 1.0E-03
HASHIMOTO THYROIDITIS, SUSCEPTIBILITY TO
0 1 0 0 1 1.0E-03
CELIAC DISEASE, SUSCEPTIBILITY TO, 3 (finding)
0 1 0 0 1 1.0E-03
CUI: C2674950
Disease: LUNG CANCER, SUSCEPTIBILITY TO
LUNG CANCER, SUSCEPTIBILITY TO
0 3 0 0 1 1.0E-03
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 2 2.1E-03
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 1.0E-03
CUI: C0004144
Disease: Atelectasis
Atelectasis
62 0 1 5.8E-04 0 0
CUI: C0158734
Disease: Polydactyly of toes
Polydactyly of toes
61 0 1 5.8E-04 0 0
CUI: C0220697
Disease: POLYDACTYLY, POSTAXIAL
POLYDACTYLY, POSTAXIAL
61 0 1 5.8E-04 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders
59 0 1 5.8E-04 0 0
CUI: C0332615
Disease: Myopathic facies
Myopathic facies
44 0 1 5.8E-04 0 0
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
43 0 1 5.8E-04 0 0
CUI: C0266631
Disease: Accessory spleen
Accessory spleen
41 0 1 5.8E-04 0 0
CUI: C4023687
Disease: EEG with multifocal slow activity
EEG with multifocal slow activity
41 0 1 5.8E-04 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination
40 0 1 5.8E-04 0 0
CUI: C3178805
Disease: Heterotaxy Syndrome
Heterotaxy Syndrome
39 0 1 5.8E-04 0 0
CUI: C4023342
Disease: Gastrostomy tube feeding in infancy
Gastrostomy tube feeding in infancy
38 0 1 5.8E-04 0 0
CUI: C0236773
Disease: Depressed bipolar I disorder
Depressed bipolar I disorder
37 0 1 5.8E-04 0 0
CUI: C0431362
Disease: Lobar Holoprosencephaly
Lobar Holoprosencephaly
37 0 1 5.8E-04 0 0
Leigh Syndrome due to Mitochondrial Complex IV Deficiency
37 0 1 5.8E-04 0 0