Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
ALZHEIMER DISEASE, SUSCEPTIBILITY TO
0 3 0 0 1 4.0E-02
VASCULAR DEMENTIA, SUSCEPTIBILITY TO
0 1 0 0 1 4.3E-02
CUI: C0042834
Disease: Vital capacity
Vital capacity
430 0 1 1.6E-03 0 0
CUI: C1850049
Disease: Clinodactyly of the 5th finger
Clinodactyly of the 5th finger
284 0 1 2.0E-03 0 0
CUI: C1314691
Disease: Age at menarche
Age at menarche
267 0 1 2.1E-03 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior
261 0 1 2.1E-03 0 0
Creatine phosphokinase serum increased
228 0 1 2.3E-03 0 0
CUI: C1857486
Disease: Low-set, posteriorly rotated ears
Low-set, posteriorly rotated ears
223 0 1 2.3E-03 0 0
CUI: C1848207
Disease: Poor speech
Poor speech
208 0 1 2.4E-03 0 0
CUI: C0040420
Disease: Tonometry
Tonometry
206 0 1 2.4E-03 0 0
CUI: C0234146
Disease: Absent reflex
Absent reflex
201 0 1 2.4E-03 0 0
CUI: C0152421
Disease: Macrotia
Macrotia
188 0 1 2.5E-03 0 0
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
187 0 1 2.5E-03 0 0
CUI: C1836047
Disease: Long face
Long face
182 0 1 2.5E-03 0 0
CUI: C0026034
Disease: Microstomia
Microstomia
172 0 1 2.6E-03 0 0
CUI: C0221352
Disease: Syndactyly of fingers
Syndactyly of fingers
171 0 1 2.6E-03 0 0
CUI: C0423224
Disease: Sunken eyes
Sunken eyes
171 0 1 2.6E-03 0 0
CUI: C0235659
Disease: Reduced fetal movement
Reduced fetal movement
169 0 1 2.6E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 1 2.6E-03 0 0
CUI: C0020796
Disease: Profound Mental Retardation
Profound Mental Retardation
160 0 1 2.7E-03 0 0
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk
156 0 1 2.7E-03 0 0
CUI: C1857679
Disease: Sloping forehead
Sloping forehead
149 0 1 2.8E-03 0 0
CUI: C0024433
Disease: Macrostomia
Macrostomia
148 0 1 2.8E-03 0 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency
148 0 1 2.8E-03 0 0
CUI: C4551485
Disease: Clinodactyly
Clinodactyly
148 0 1 2.8E-03 0 0