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: C0740302
Disease: 5q-syndrome
5q-syndrome
45 0 1 2.1E-02 0 0
CUI: C1563730
Disease: Abdominal Cryptorchidism
Abdominal Cryptorchidism
8 0 1 9.1E-02 0 0
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 1 6.2E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.3E-03 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 2 2.2E-03 0 0
CUI: C0349705
Disease: Abnormal hemoglobin finding
Abnormal hemoglobin finding
9 0 1 8.3E-02 0 0
CUI: C0855742
Disease: Abnormal platelet morphology
Abnormal platelet morphology
10 0 1 7.7E-02 0 0
Abnormal pulmonary valve cusp morphology
2 0 1 0.20 0 0
Abnormal serum dehydroepiandrosterone level
1 0 1 0.25 0 0
Abnormality of blood and blood-forming tissues
23 0 1 3.8E-02 0 0
CUI: C1846821
Disease: Abnormality of coagulation
Abnormality of coagulation
59 0 1 1.6E-02 0 0
CUI: C4020755
Disease: Abnormality of fontanelles
Abnormality of fontanelles
3 0 1 0.17 0 0
Abnormality of metabolism/homeostasis
171 0 2 1.2E-02 0 0
Abnormality of reproductive system physiology
1 0 1 0.25 0 0
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition
140 0 1 7.0E-03 0 0
CUI: C0281842
Disease: Abnormality of the fallopian tube
Abnormality of the fallopian tube
22 0 1 4.0E-02 0 0
Abnormality of the femoral metaphysis
4 0 1 0.14 0 0
CUI: C4025814
Disease: Abnormality of the metaphysis
Abnormality of the metaphysis
97 0 1 1.0E-02 0 0
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system
148 0 1 6.6E-03 0 0
Abnormality of the tibial metaphysis
3 0 1 0.17 0 0
CUI: C0878638
Disease: Abnormality of the tongue
Abnormality of the tongue
25 0 1 3.6E-02 0 0
CUI: C4025655
Disease: Abnormality of urine homeostasis
Abnormality of urine homeostasis
1 0 1 0.25 0 0
CUI: C0267756
Disease: Abscess of peritoneum
Abscess of peritoneum
9 0 1 8.3E-02 0 0
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy
89 0 1 1.1E-02 0 0
CUI: C1855669
Disease: Absent frontal sinuses
Absent frontal sinuses
9 0 1 8.3E-02 0 0