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: C0026826
Disease: Muscle Hypertonia
Muscle Hypertonia
197 0 1 2.1E-03 0 0
CUI: C0037822
Disease: Speech Disorders
Speech Disorders
183 0 1 2.1E-03 0 0
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge
180 0 1 2.2E-03 0 0
CUI: C1836440
Disease: Increased serum lactate
Increased serum lactate
169 0 1 2.2E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 0 1 2.3E-03 0 0
CUI: C1857679
Disease: Sloping forehead
Sloping forehead
149 0 1 2.3E-03 0 0
CUI: C0004106
Disease: Astigmatism
Astigmatism
148 0 1 2.3E-03 0 0
CUI: C0266551
Disease: Congenital coloboma of iris
Congenital coloboma of iris
148 0 1 2.3E-03 0 0
CUI: C1858430
Disease: Death in infancy
Death in infancy
146 0 1 2.3E-03 0 0
CUI: C0020490
Disease: Hyperopia
Hyperopia
142 0 1 2.3E-03 0 0
CUI: C0003466
Disease: Anus, Imperforate
Anus, Imperforate
139 0 1 2.4E-03 0 0
CUI: C0152423
Disease: Congenital small ears
Congenital small ears
137 0 1 2.4E-03 0 0
CUI: C1849089
Disease: Broad forehead
Broad forehead
133 0 1 2.4E-03 0 0
CUI: C0518015
Disease: Hemoglobin measurement
Hemoglobin measurement
131 0 1 2.4E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color
130 0 1 2.4E-03 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause
129 0 1 2.4E-03 0 0
CUI: C0234162
Disease: Cerebellar Dysmetria
Cerebellar Dysmetria
127 0 1 2.4E-03 0 0
Creatinine measurement, serum (procedure)
124 0 1 2.5E-03 0 0
CUI: C0014877
Disease: Esotropia
Esotropia
121 0 1 2.5E-03 0 0
Sensorineural hearing loss, bilateral
117 0 1 2.5E-03 0 0
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity
113 0 1 2.5E-03 0 0
CUI: C0375206
Disease: Hemiplegia/hemiparesis
Hemiplegia/hemiparesis
112 0 1 2.5E-03 0 0
CUI: C1837770
Disease: Sparse hair
Sparse hair
112 0 1 2.5E-03 0 0
CUI: C1835884
Disease: Triangular face
Triangular face
111 0 1 2.5E-03 0 0
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
109 0 1 2.5E-03 0 0