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
Abdominal obesity metabolic syndrome
10 0 1 6.7E-02 0 0
CUI: C0522216
Disease: Abnormal auditory evoked potential
Abnormal auditory evoked potential
11 0 2 0.13 0 0
CUI: C0233514
Disease: Abnormal behavior
Abnormal behavior
910 0 1 1.1E-03 0 0
CUI: C4476724
Disease: Abnormal cellular phenotype
Abnormal cellular phenotype
4 0 1 0.11 0 0
CUI: C4023607
Disease: Abnormal corpus striatum morphology
Abnormal corpus striatum morphology
5 0 1 1.0E-01 0 0
CUI: C4025252
Disease: Abnormal nasal morphology
Abnormal nasal morphology
34 0 1 2.6E-02 0 0
CUI: C0497202
Disease: Abnormal ocular motility
Abnormal ocular motility
45 0 1 2.0E-02 0 0
CUI: C4025887
Disease: Abnormal oral cavity morphology
Abnormal oral cavity morphology
12 0 1 5.9E-02 0 0
CUI: C4025648
Disease: Abnormal peripheral myelination
Abnormal peripheral myelination
2 0 1 0.14 0 0
CUI: C1260926
Disease: Abnormal pigmentation
Abnormal pigmentation
58 0 3 4.9E-02 0 0
CUI: C4020957
Disease: Abnormal trabecular bone morphology
Abnormal trabecular bone morphology
6 0 1 9.1E-02 0 0
Abnormal upper motor neuron morphology
20 0 1 4.0E-02 0 0
CUI: C3665386
Disease: Abnormal vision
Abnormal vision
115 0 1 8.3E-03 0 0
CUI: C0522214
Disease: Abnormal visual evoked potential
Abnormal visual evoked potential
55 0 2 3.4E-02 0 0
CUI: C4025692
Disease: Abnormality of calvarial morphology
Abnormality of calvarial morphology
8 0 1 7.7E-02 0 0
Abnormality of cardiovascular system morphology
198 0 1 4.9E-03 0 0
CUI: C4023722
Disease: Abnormality of hair texture
Abnormality of hair texture
15 0 1 5.0E-02 0 0
Abnormality of immune system physiology
42 0 1 2.1E-02 0 0
CUI: C4021755
Disease: Abnormality of midbrain morphology
Abnormality of midbrain morphology
2 0 1 0.14 0 0
Abnormality of ocular smooth pursuit
5 0 1 1.0E-01 0 0
CUI: C1862475
Disease: Abnormality of retinal pigmentation
Abnormality of retinal pigmentation
215 0 1 4.5E-03 0 0
Abnormality of skeletal muscle fiber size
8 0 1 7.7E-02 0 0
CUI: C4520981
Disease: Abnormality of the basal ganglia
Abnormality of the basal ganglia
17 0 1 4.5E-02 0 0
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition
140 0 1 6.9E-03 0 0