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: C0004158
Disease: Athetosis
Athetosis
0 3 0 0 1 1.0E-01
CUI: C0008489
Disease: Chorea
Chorea
0 20 0 0 1 3.7E-02
CUI: C0026961
Disease: Mydriasis
Mydriasis
0 2 0 0 1 0.11
CUI: C0030232
Disease: Pallor
Pallor
0 4 0 0 1 9.1E-02
CUI: C0240595
Disease: Rotary Nystagmus
Rotary Nystagmus
0 3 0 0 1 1.0E-01
CUI: C0267071
Disease: Oropharyngeal Dysphagia
Oropharyngeal Dysphagia
0 8 0 0 1 6.7E-02
CUI: C0546884
Disease: Hypovolemia
Hypovolemia
0 3 0 0 1 1.0E-01
CUI: C0576225
Disease: Long foot
Long foot
0 3 0 0 1 1.0E-01
CUI: C1837732
Disease: Thickened helices
Thickened helices
0 3 0 0 1 1.0E-01
Primitive reflexes (palmomental, snout, glabellar)
0 1 0 0 1 0.12
CUI: C1839783
Disease: Large forehead
Large forehead
0 1 0 0 1 0.12
CUI: C1842060
Disease: Prominent supraorbital ridges
Prominent supraorbital ridges
0 10 0 0 1 5.9E-02
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2
0 10 0 0 1 5.9E-02
CUI: C1845274
Disease: Abnormal conjugate eye movement
Abnormal conjugate eye movement
0 5 0 0 1 8.3E-02
CUI: C1849043
Disease: Soft, doughy skin
Soft, doughy skin
0 4 0 0 1 9.1E-02
CUI: C1859481
Disease: Abnormal finger flexion creases
Abnormal finger flexion creases
0 1 0 0 1 0.12
CUI: C1969810
Disease: FEBRILE CONVULSIONS, FAMILIAL, 8
FEBRILE CONVULSIONS, FAMILIAL, 8
0 13 0 0 1 5.0E-02
CUI: C3810018
Disease: Bilateral coxa valga
Bilateral coxa valga
0 3 0 0 1 1.0E-01
CUI: C4021603
Disease: Widely spaced primary teeth
Widely spaced primary teeth
0 1 0 0 1 0.12
CUI: C4023422
Disease: Long palm
Long palm
0 2 0 0 1 0.11
Abnormality of the vertebral spinous processes
0 1 0 0 1 0.12
CUI: C4048268
Disease: Cortical visual impairment
Cortical visual impairment
0 27 0 0 1 2.9E-02
CUI: C4072908
Disease: Induced vaginal delivery
Induced vaginal delivery
0 10 0 0 1 5.9E-02
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.2E-03 0 0
CUI: C0001080
Disease: Achondroplasia
Achondroplasia
46 0 1 1.6E-02 0 0