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 3.6E-03
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 2 7.1E-03
CUI: C0752138
Disease: Intracranial Arterial Diseases
Intracranial Arterial Diseases
0 1 0 0 1 3.6E-03
CUI: C0863104
Disease: Neck discomfort
Neck discomfort
0 2 0 0 1 3.5E-03
CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO
0 1 0 0 1 3.6E-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 3.6E-03
Frequent episodic tension-type headache
0 1 0 0 1 3.6E-03
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 2 7.1E-03
CUI: C0018520
Disease: Halitosis
Halitosis
48 0 1 4.8E-04 0 0
CUI: C1854387
Disease: Type 1 muscle fiber predominance
Type 1 muscle fiber predominance
44 0 1 4.8E-04 0 0
Ciliary Dyskinesia, Primary, 1, With Or Without Situs Inversus
43 0 1 4.8E-04 0 0
CUI: C0154860
Disease: Hereditary retinal dystrophy
Hereditary retinal dystrophy
42 0 1 4.8E-04 0 0
CUI: C0234860
Disease: Weak cry
Weak cry
42 0 1 4.8E-04 0 0
CUI: C1859470
Disease: Large basal ganglia
Large basal ganglia
41 0 1 4.8E-04 0 0
Decreased activity of mitochondrial complex I
41 0 1 4.8E-04 0 0
CUI: C4023687
Disease: EEG with multifocal slow activity
EEG with multifocal slow activity
41 0 1 4.8E-04 0 0
CUI: C0200695
Disease: Fetal hemoglobin determination
Fetal hemoglobin determination
40 0 1 4.8E-04 0 0
CUI: C1838979
Disease: MITOCHONDRIAL COMPLEX I DEFICIENCY
MITOCHONDRIAL COMPLEX I DEFICIENCY
40 0 1 4.8E-04 0 0
CUI: C0427063
Disease: Shoulder girdle weakness
Shoulder girdle weakness
39 0 1 4.8E-04 0 0
CUI: C4022738
Disease: Neurodevelopmental delay
Neurodevelopmental delay
39 0 1 4.8E-04 0 0
CUI: C1838705
Disease: Anteriorly placed anus
Anteriorly placed anus
34 0 1 4.8E-04 0 0
CUI: C4024923
Disease: Diffuse white matter abnormalities
Diffuse white matter abnormalities
34 0 1 4.8E-04 0 0
CUI: C4228778
Disease: Abnormality of radial ray
Abnormality of radial ray
34 0 1 4.8E-04 0 0
Focal T2 hyperintense brainstem lesion
33 0 1 4.8E-04 0 0