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: C0852654
Disease: 21-hydroxylase deficiency
21-hydroxylase deficiency
55 0 2 2.3E-02 0 0
6-Phosphogluconolactonase Deficiency
1 0 1 3.0E-02 0 0
6-pyruvoyl-tetrahydropterin synthase deficiency
5 0 1 2.7E-02 0 0
CUI: C0000731
Disease: Abdomen distended
Abdomen distended
103 0 1 7.4E-03 0 0
CUI: C0000735
Disease: Abdominal Neoplasms
Abdominal Neoplasms
13 0 1 2.2E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 5 1.5E-02 0 0
CUI: C0000744
Disease: Abetalipoproteinemia
Abetalipoproteinemia
65 0 1 1.0E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 6 6.4E-03 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
59 0 1 1.1E-02 0 0
CUI: C0278061
Disease: Abnormal mental state
Abnormal mental state
24 0 1 1.8E-02 0 0
CUI: C0852413
Disease: Abnormal muscle tone
Abnormal muscle tone
14 0 1 2.2E-02 0 0
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation
58 0 1 1.1E-02 0 0
CUI: C4551596
Disease: Abnormal renal morphology
Abnormal renal morphology
35 0 1 1.5E-02 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision
115 0 1 6.8E-03 0 0
Abnormality of metabolism/homeostasis
171 0 3 1.5E-02 0 0
CUI: C4021755
Disease: Abnormality of midbrain morphology
Abnormality of midbrain morphology
2 0 1 2.9E-02 0 0
Abnormality of pelvic girdle bone morphology
55 0 1 1.1E-02 0 0
CUI: C1866129
Disease: Abnormality of the cerebellum
Abnormality of the cerebellum
55 0 1 1.1E-02 0 0
CUI: C4025362
Disease: Abnormality of the gastric mucosa
Abnormality of the gastric mucosa
12 0 1 2.3E-02 0 0
CUI: C4021753
Disease: Abnormality of the immune system
Abnormality of the immune system
34 0 1 1.5E-02 0 0
CUI: C4025814
Disease: Abnormality of the metaphysis
Abnormality of the metaphysis
97 0 1 7.8E-03 0 0
CUI: C4021818
Disease: Abnormality of the ovary
Abnormality of the ovary
8 0 1 2.5E-02 0 0
Abnormality of the respiratory system
16 0 1 2.1E-02 0 0
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system
148 0 2 1.1E-02 0 0
CUI: C0860218
Disease: ABO incompatibility
ABO incompatibility
14 2 4 9.3E-02 1 0.33