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 1 1.3E-02 0 0
Abdominal obesity metabolic syndrome
10 0 1 3.3E-02 0 0
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 5 1.6E-02 0 0
CUI: C0740651
Disease: Abdominal symptom
Abdominal symptom
17 0 1 2.7E-02 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 2 2.2E-03 0 0
CUI: C2132198
Disease: Abnormal blistering of the skin
Abnormal blistering of the skin
75 0 1 1.1E-02 0 0
CUI: C4025836
Disease: Abnormal choroid morphology
Abnormal choroid morphology
12 0 1 3.1E-02 0 0
CUI: C4022922
Disease: Abnormal enzyme/coenzyme activity
Abnormal enzyme/coenzyme activity
13 0 1 3.0E-02 0 0
CUI: C1857704
Disease: Abnormal myelination
Abnormal myelination
49 0 2 2.9E-02 0 0
CUI: C1837388
Disease: Abnormal pattern of respiration
Abnormal pattern of respiration
20 0 2 5.1E-02 0 0
CUI: C0151746
Disease: Abnormal renal function
Abnormal renal function
12 0 1 3.1E-02 0 0
CUI: C4025840
Disease: Abnormal sclera morphology
Abnormal sclera morphology
1 0 1 4.8E-02 0 0
CUI: C1839341
Disease: Abnormal T-wave
Abnormal T-wave
20 0 2 5.1E-02 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision
115 0 1 7.4E-03 0 0
CUI: C4280760
Disease: Abnormal visual accommodation
Abnormal visual accommodation
5 0 1 4.0E-02 0 0
CUI: C4021800
Disease: Abnormality of dental enamel
Abnormality of dental enamel
96 0 1 8.6E-03 0 0
CUI: C4073214
Disease: Abnormality of masseter muscle
Abnormality of masseter muscle
2 0 1 4.5E-02 0 0
Abnormality of metabolism/homeostasis
171 0 1 5.2E-03 0 0
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
28 0 1 2.1E-02 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 1 4.3E-03 0 0
CUI: C4025814
Disease: Abnormality of the metaphysis
Abnormality of the metaphysis
97 0 1 8.5E-03 0 0
CUI: C4023042
Disease: Abnormality of the mitochondrion
Abnormality of the mitochondrion
10 0 1 3.3E-02 0 0
CUI: C1846460
Disease: Abnormality of the outer ear
Abnormality of the outer ear
95 0 1 8.7E-03 0 0
CUI: C4317107
Disease: Abnormality of the thyroid gland
Abnormality of the thyroid gland
21 0 1 2.4E-02 0 0
CUI: C0014553
Disease: Absence Epilepsy
Absence Epilepsy
89 0 1 9.2E-03 0 0