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: C0002940
Disease: Aneurysm
Aneurysm
22 36 4 4.8E-02 5 0.12
CUI: C0023890
Disease: Liver Cirrhosis
Liver Cirrhosis
1182 189 33 2.7E-02 5 2.6E-02
CUI: C0270685
Disease: Cerebral calcification
Cerebral calcification
103 8 9 5.6E-02 5 0.42
CUI: C3150910
Disease: Brain calcification Rajab type
Brain calcification Rajab type
1 10 1 1.5E-02 5 0.36
CUI: C0002390
Disease: Extrinsic allergic alveolitis
Extrinsic allergic alveolitis
65 2 21 0.19 2 0.22
CUI: C0009782
Disease: Connective Tissue Diseases
Connective Tissue Diseases
188 24 15 6.3E-02 2 6.5E-02
Persistent Fetal Circulation Syndrome
14 7 3 3.9E-02 2 0.14
CUI: C1800706
Disease: Idiopathic Pulmonary Fibrosis
Idiopathic Pulmonary Fibrosis
803 63 43 5.2E-02 2 2.9E-02
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
2723 2387 40 1.5E-02 1 4.2E-04
CUI: C0006267
Disease: Bronchiectasis
Bronchiectasis
190 15 22 9.4E-02 1 4.3E-02
CUI: C0010709
Disease: Cyst
Cyst
221 6 12 4.4E-02 1 7.1E-02
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
967 579 5 4.9E-03 1 1.7E-03
CUI: C0034069
Disease: Pulmonary Fibrosis
Pulmonary Fibrosis
924 25 40 4.2E-02 1 3.0E-02
CUI: C0036421
Disease: Systemic Scleroderma
Systemic Scleroderma
979 287 32 3.2E-02 1 3.4E-03
CUI: C0042580
Disease: Vesico-Ureteral Reflux
Vesico-Ureteral Reflux
187 23 6 2.4E-02 1 3.2E-02
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial
319 144 33 9.4E-02 1 6.6E-03
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH)
1075 276 25 2.2E-02 1 3.5E-03
CUI: C1837260
Disease: Prominent forehead
Prominent forehead
159 25 2 9.0E-03 1 3.0E-02
PULMONARY FIBROSIS, IDIOPATHIC, SUSCEPTIBILITY TO
0 1 0 0 1 0.11
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver
75 8 2 1.4E-02 1 6.2E-02
CUI: C4531138
Disease: Short telomere length
Short telomere length
12 1 4 5.4E-02 1 0.11
CUI: C4721509
Disease: Usual Interstitial Pneumonia
Usual Interstitial Pneumonia
64 2 18 0.16 1 1.0E-01
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 6 1.7E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 2 1.6E-02 0 0
CUI: C0000768
Disease: Congenital Abnormality
Congenital Abnormality
1098 0 17 1.5E-02 0 0