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 0.20
CUI: C0026961
Disease: Mydriasis
Mydriasis
0 2 0 0 1 0.25
CUI: C0030232
Disease: Pallor
Pallor
0 4 0 0 1 0.17
CUI: C0240595
Disease: Rotary Nystagmus
Rotary Nystagmus
0 3 0 0 1 0.20
CUI: C0426209
Disease: amniotic fluid meconium stained
amniotic fluid meconium stained
0 4 0 0 1 0.17
CUI: C0546884
Disease: Hypovolemia
Hypovolemia
0 3 0 0 1 0.20
CUI: C1328407
Disease: Hip Dysplasia
Hip Dysplasia
0 16 0 0 1 5.6E-02
Primitive reflexes (palmomental, snout, glabellar)
0 1 0 0 1 0.33
EPILEPSY, CHILDHOOD ABSENCE, SUSCEPTIBILITY TO, 2
0 10 0 0 1 8.3E-02
CUI: C1844820
Disease: Range of joint movement increased
Range of joint movement increased
0 46 0 0 1 2.1E-02
CUI: C1845274
Disease: Abnormal conjugate eye movement
Abnormal conjugate eye movement
0 5 0 0 1 0.14
CUI: C1849043
Disease: Soft, doughy skin
Soft, doughy skin
0 4 0 0 1 0.17
CUI: C1850629
Disease: Exaggerated cupid's bow
Exaggerated cupid's bow
0 6 0 0 1 0.12
CUI: C1857479
Disease: Short columella
Short columella
0 5 0 0 1 0.14
CUI: C1859481
Disease: Abnormal finger flexion creases
Abnormal finger flexion creases
0 1 0 0 1 0.33
CUI: C1969810
Disease: FEBRILE CONVULSIONS, FAMILIAL, 8
FEBRILE CONVULSIONS, FAMILIAL, 8
0 13 0 0 1 6.7E-02
CUI: C3150613
Disease: Long toe
Long toe
0 8 0 0 1 1.0E-01
CUI: C3697248
Disease: Short lower third of face
Short lower third of face
0 3 0 0 1 0.20
CUI: C3810018
Disease: Bilateral coxa valga
Bilateral coxa valga
0 3 0 0 1 0.20
CUI: C4021603
Disease: Widely spaced primary teeth
Widely spaced primary teeth
0 1 0 0 1 0.33
Abnormality of the vertebral spinous processes
0 1 0 0 1 0.33
CUI: C0000737
Disease: Abdominal Pain
Abdominal Pain
302 0 1 3.1E-03 0 0
CUI: C0000846
Disease: Agenesis
Agenesis
161 0 1 5.4E-03 0 0
CUI: C0001311
Disease: Acute bronchiolitis
Acute bronchiolitis
11 0 1 2.9E-02 0 0
CUI: C0001430
Disease: Adenoma
Adenoma
1183 0 1 8.3E-04 0 0