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: C4551570
Disease: 2-3 toe syndactyly
2-3 toe syndactyly
85 0 1 1.1E-02 0 0
CUI: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 1 1.6E-02 0 0
CUI: C0549357
Disease: Abdominal adhesions
Abdominal adhesions
6 0 1 6.7E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.2E-03 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 1 1.4E-02 0 0
CUI: C1860224
Disease: ABLEPHARON-MACROSTOMIA SYNDROME
ABLEPHARON-MACROSTOMIA SYNDROME
41 0 1 2.0E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 5 5.5E-03 0 0
CUI: C4011556
Disease: Abnormal eyebrow morphology
Abnormal eyebrow morphology
29 0 1 2.6E-02 0 0
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation
58 0 1 1.5E-02 0 0
CUI: C4021087
Disease: Abnormal social behavior
Abnormal social behavior
19 0 1 3.6E-02 0 0
CUI: C4021611
Disease: Abnormality of epiphysis morphology
Abnormality of epiphysis morphology
86 0 1 1.1E-02 0 0
Abnormality of female internal genitalia
31 0 1 2.5E-02 0 0
CUI: C4025034
Disease: Abnormality of femoral epiphysis
Abnormality of femoral epiphysis
1 0 1 1.0E-01 0 0
Abnormality of immune system physiology
42 0 1 2.0E-02 0 0
Abnormality of mitochondrial metabolism
21 0 1 3.3E-02 0 0
Abnormality of pelvic girdle bone morphology
55 0 1 1.6E-02 0 0
CUI: C4021664
Disease: Abnormality of the abdominal wall
Abnormality of the abdominal wall
17 0 1 3.8E-02 0 0
CUI: C1866129
Disease: Abnormality of the cerebellum
Abnormality of the cerebellum
55 0 1 1.6E-02 0 0
Abnormality of the cerebrospinal fluid
3 0 1 8.3E-02 0 0
CUI: C4021780
Disease: Abnormality of the liver
Abnormality of the liver
75 0 1 1.2E-02 0 0
CUI: C4025814
Disease: Abnormality of the metaphysis
Abnormality of the metaphysis
97 0 1 9.4E-03 0 0
CUI: C4025750
Disease: Abnormality of the nasopharynx
Abnormality of the nasopharynx
10 0 1 5.3E-02 0 0
Abnormality of the periventricular white matter
45 0 1 1.9E-02 0 0
CUI: C4025838
Disease: Abnormality of the pharynx
Abnormality of the pharynx
23 0 1 3.1E-02 0 0
Abnormality of the respiratory system
16 0 1 4.0E-02 0 0