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: C0339619
Disease: Congenital esotropia
Congenital esotropia
0 2 0 0 1 6.7E-02
Breast Diffuse Large B-Cell Lymphoma
0 1 0 0 1 7.1E-02
CUI: C0034935
Disease: Babinski Reflex
Babinski Reflex
218 0 1 2.3E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 1 2.3E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
176 0 1 2.5E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 1 2.5E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control
162 0 1 2.6E-03 0 0
CUI: C0476397
Disease: Electroretinogram abnormal
Electroretinogram abnormal
158 0 1 2.6E-03 0 0
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk
156 0 1 2.6E-03 0 0
CUI: C0221358
Disease: Long narrow head
Long narrow head
154 0 1 2.6E-03 0 0
CUI: C0684276
Disease: Hypsarrhythmia
Hypsarrhythmia
152 0 1 2.6E-03 0 0
CUI: C0231686
Disease: Gait, Unsteady
Gait, Unsteady
143 0 1 2.7E-03 0 0
CUI: C0005938
Disease: Bone Density
Bone Density
138 0 1 2.7E-03 0 0
Platelet Component Distribution Width Measurement
134 0 1 2.8E-03 0 0
CUI: C1629609
Disease: Age at menopause
Age at menopause
129 0 1 2.8E-03 0 0
Creatinine measurement, serum (procedure)
124 0 1 2.9E-03 0 0
CUI: C0014877
Disease: Esotropia
Esotropia
121 0 1 2.9E-03 0 0
CUI: C0431380
Disease: Cortical Dysplasia
Cortical Dysplasia
118 0 1 2.9E-03 0 0
CUI: C1837658
Disease: Gross motor development delay
Gross motor development delay
118 0 1 2.9E-03 0 0
CUI: C1860834
Disease: Infantile muscular hypotonia
Infantile muscular hypotonia
118 0 1 2.9E-03 0 0
Sensorineural hearing loss, bilateral
117 0 1 2.9E-03 0 0
CUI: C0576093
Disease: Knee joint valgus deformity
Knee joint valgus deformity
117 0 1 2.9E-03 0 0
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity
113 0 1 2.9E-03 0 0
CUI: C1277241
Disease: Delayed myelination
Delayed myelination
112 0 1 3.0E-03 0 0
CUI: C3161330
Disease: Profound intellectual disabilities
Profound intellectual disabilities
112 0 1 3.0E-03 0 0