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: C0750880
Disease: Monocyte count result
Monocyte count result
139 0 1 3.3E-03 0 0
CUI: C0005938
Disease: Bone Density
Bone Density
138 0 1 3.3E-03 0 0
Platelet Component Distribution Width Measurement
134 0 1 3.4E-03 0 0
CUI: C0266544
Disease: Microcornea
Microcornea
129 0 1 3.4E-03 0 0
CUI: C0039075
Disease: Syndactyly
Syndactyly
127 0 1 3.5E-03 0 0
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision
127 0 1 3.5E-03 0 0
CUI: C0685409
Disease: Congenital Camptodactyly
Congenital Camptodactyly
123 0 1 3.5E-03 0 0
CUI: C0014877
Disease: Esotropia
Esotropia
121 0 1 3.5E-03 0 0
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly
120 0 1 3.6E-03 0 0
Childhood T Acute Lymphoblastic Leukemia
119 0 1 3.6E-03 0 0
CUI: C1860834
Disease: Infantile muscular hypotonia
Infantile muscular hypotonia
118 0 1 3.6E-03 0 0
Sensorineural hearing loss, bilateral
117 0 1 3.6E-03 0 0
CUI: C1842876
Disease: Depressed nasal ridge
Depressed nasal ridge
117 0 1 3.6E-03 0 0
CUI: C0576226
Disease: Short foot
Short foot
116 0 1 3.6E-03 0 0
Aplasia/Hypoplasia of the cerebellum
116 0 1 3.6E-03 0 0
CUI: C0024421
Disease: Macroglossia
Macroglossia
115 0 1 3.6E-03 0 0
CUI: C4021726
Disease: EMG: myopathic abnormalities
EMG: myopathic abnormalities
115 0 1 3.6E-03 0 0
CUI: C0037369
Disease: Smoking
Smoking
391 0 2 3.6E-03 0 0
CUI: C0266617
Disease: Congenital anomaly of face
Congenital anomaly of face
114 0 1 3.6E-03 0 0
CUI: C0231712
Disease: Waddling gait
Waddling gait
113 0 1 3.6E-03 0 0
CUI: C3495676
Disease: Anorectal Malformations
Anorectal Malformations
112 0 1 3.7E-03 0 0
CUI: C0431447
Disease: Synophrys
Synophrys
111 0 1 3.7E-03 0 0
CUI: C0005823
Disease: Blood Pressure
Blood Pressure
109 0 1 3.7E-03 0 0
CUI: C0240340
Disease: Microdontia (disorder)
Microdontia (disorder)
109 0 1 3.7E-03 0 0
CUI: C1963167
Disease: Memory Impairment, CTCAE 3.0
Memory Impairment, CTCAE 3.0
109 0 1 3.7E-03 0 0