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: C4023736
Disease: 2-5 finger syndactyly
2-5 finger syndactyly
1 0 1 9.1E-02 0 0
CUI: C4023731
Disease: 4-5 finger syndactyly
4-5 finger syndactyly
3 0 1 7.7E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 2 6.4E-03 0 0
CUI: C4022916
Disease: Abnormal aldolase level
Abnormal aldolase level
16 0 5 0.23 0 0
CUI: C0266781
Disease: Abnormal amniotic fluid
Abnormal amniotic fluid
8 0 1 5.6E-02 0 0
CUI: C4476793
Disease: Abnormal cell morphology
Abnormal cell morphology
12 0 1 4.5E-02 0 0
CUI: C1856019
Disease: Abnormal cortical gyration
Abnormal cortical gyration
17 0 1 3.7E-02 0 0
Abnormal isoelectric focusing of serum transferrin
15 0 1 4.0E-02 0 0
Abnormal lactate dehydrogenase activity
19 0 5 0.20 0 0
Abnormal liver parenchyma morphology
4 0 1 7.1E-02 0 0
CUI: C4022707
Disease: Abnormal scrotal rugation
Abnormal scrotal rugation
4 0 1 7.1E-02 0 0
Abnormal subcutaneous fat tissue distribution
9 0 1 5.3E-02 0 0
CUI: C4025845
Disease: Abnormality iris morphology
Abnormality iris morphology
27 0 6 0.19 0 0
CUI: C4021085
Disease: Abnormality of brain morphology
Abnormality of brain morphology
104 0 3 2.7E-02 0 0
Abnormality of metabolism/homeostasis
171 0 1 5.5E-03 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 1 4.4E-03 0 0
CUI: C4021642
Disease: Abnormality of the Achilles tendon
Abnormality of the Achilles tendon
8 0 1 5.6E-02 0 0
CUI: C4025871
Disease: Abnormality of the face
Abnormality of the face
31 0 1 2.4E-02 0 0
CUI: C4022964
Disease: Abnormality of the occipital bone
Abnormality of the occipital bone
4 0 1 7.1E-02 0 0
CUI: C1846460
Disease: Abnormality of the outer ear
Abnormality of the outer ear
95 0 1 9.5E-03 0 0
Abnormality of the periventricular white matter
45 0 6 0.12 0 0
CUI: C0857379
Disease: Abnormality of the pinna
Abnormality of the pinna
85 0 1 1.1E-02 0 0
CUI: C4024905
Disease: Abnormality of the pons
Abnormality of the pons
7 0 4 0.29 0 0
Abnormality of the spinocerebellar tracts
3 0 1 7.7E-02 0 0
CUI: C4022403
Disease: Abnormality of the substantia nigra
Abnormality of the substantia nigra
3 0 1 7.7E-02 0 0