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 1.4E-02
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 9 0 0 1 1.3E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 1.4E-02
CUI: C0341479
Disease: Infected pancreatic necrosis
Infected pancreatic necrosis
0 2 0 0 1 1.4E-02
Multi vessel coronary artery disease
0 1 0 0 1 1.4E-02
ALZHEIMER DISEASE, SUSCEPTIBILITY TO
0 3 0 0 1 1.4E-02
CORONARY ARTERY DISEASE, SEVERE, SUSCEPTIBILITY TO
0 1 0 0 1 1.4E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 1.4E-02
CUI: C3899405
Disease: Decreased Attention
Decreased Attention
0 3 0 0 1 1.4E-02
VASCULAR DEMENTIA, SUSCEPTIBILITY TO
0 1 0 0 1 1.4E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 2 2.9E-02
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 0 1 2.5E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color
130 0 1 2.7E-03 0 0
CUI: C0236969
Disease: Substance-Related Disorders
Substance-Related Disorders
128 0 1 2.7E-03 0 0
CUI: C1866195
Disease: Downturned corners of mouth
Downturned corners of mouth
122 0 1 2.8E-03 0 0
CUI: C0013222
Disease: Drug Use Disorders
Drug Use Disorders
121 0 1 2.8E-03 0 0
CUI: C3714581
Disease: Multicystic Dysplastic Kidney
Multicystic Dysplastic Kidney
121 0 1 2.8E-03 0 0
CUI: C1277241
Disease: Delayed myelination
Delayed myelination
112 0 1 2.8E-03 0 0
Congenital absence of kidneys syndrome
110 0 1 2.9E-03 0 0
CUI: C4021759
Disease: Generalized myoclonic seizures
Generalized myoclonic seizures
105 0 1 2.9E-03 0 0
CUI: C4551493
Disease: Situs inversus totalis
Situs inversus totalis
104 0 1 2.9E-03 0 0
CUI: C4021786
Disease: Atypical scarring of skin
Atypical scarring of skin
101 0 1 2.9E-03 0 0
CUI: C0857490
Disease: Granulocyte count
Granulocyte count
100 0 1 2.9E-03 0 0
CUI: C0578038
Disease: Thin lips
Thin lips
99 0 1 2.9E-03 0 0
CUI: C0554970
Disease: Pallor of optic disc
Pallor of optic disc
98 0 1 3.0E-03 0 0