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 1.0E-02 0 0
CUI: C0740302
Disease: 5q-syndrome
5q-syndrome
45 0 1 1.8E-02 0 0
Abnormal brainstem MRI signal intensity
5 0 1 5.9E-02 0 0
CUI: C0520966
Disease: Abnormal coordination
Abnormal coordination
59 0 2 2.9E-02 0 0
CUI: C1856019
Disease: Abnormal cortical gyration
Abnormal cortical gyration
17 0 1 3.4E-02 0 0
CUI: C4022855
Disease: Abnormal involuntary eye movements
Abnormal involuntary eye movements
6 0 1 5.6E-02 0 0
Abnormal lower motor neuron morphology
23 0 1 2.9E-02 0 0
CUI: C4476625
Disease: Abnormal temper tantrums
Abnormal temper tantrums
4 0 1 6.2E-02 0 0
Abnormal thalamic MRI signal intensity
4 0 1 6.2E-02 0 0
CUI: C4025678
Disease: Abnormal trachea morphology
Abnormal trachea morphology
2 0 1 7.1E-02 0 0
Abnormal upper motor neuron morphology
20 0 1 3.1E-02 0 0
CUI: C0522214
Disease: Abnormal visual evoked potential
Abnormal visual evoked potential
55 0 1 1.5E-02 0 0
Abnormality of cardiovascular system morphology
198 0 2 9.6E-03 0 0
CUI: C4025843
Disease: Abnormality of refraction
Abnormality of refraction
28 0 1 2.5E-02 0 0
CUI: C4021779
Disease: Abnormality of the calf musculature
Abnormality of the calf musculature
9 0 1 4.8E-02 0 0
CUI: C0262444
Disease: Abnormality of the dentition
Abnormality of the dentition
140 0 1 6.6E-03 0 0
Abnormality of the extraocular muscles
4 0 1 6.2E-02 0 0
CUI: C1856660
Disease: Abnormality of the helix
Abnormality of the helix
21 0 1 3.0E-02 0 0
CUI: C4025750
Disease: Abnormality of the nasopharynx
Abnormality of the nasopharynx
10 0 2 9.5E-02 0 0
CUI: C4021790
Disease: Abnormality of the skeletal system
Abnormality of the skeletal system
148 0 1 6.3E-03 0 0
Abnormality of the temporomandibular joint
4 0 1 6.2E-02 0 0
CUI: C1840382
Disease: Abnormality of the ureter
Abnormality of the ureter
19 0 1 3.2E-02 0 0
CUI: C4316903
Disease: Absence Seizures
Absence Seizures
205 0 1 4.6E-03 0 0
CUI: C4021055
Disease: Absent muscle fiber merosin
Absent muscle fiber merosin
1 0 1 7.7E-02 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 2 9.4E-03 0 0