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: C1314691
Disease: Age at menarche
Age at menarche
267 0 1 1.9E-03 0 0
CUI: C0856975
Disease: Autistic behavior
Autistic behavior
261 0 1 2.0E-03 0 0
Creatine phosphokinase serum increased
228 0 1 2.1E-03 0 0
CUI: C3494422
Disease: Retrognathia
Retrognathia
191 0 1 2.3E-03 0 0
CUI: C1854113
Disease: Prominent nasal bridge
Prominent nasal bridge
180 0 1 2.3E-03 0 0
CUI: C0751837
Disease: Gait Ataxia
Gait Ataxia
172 0 1 2.4E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 1 2.4E-03 0 0
COLORECTAL CANCER, SUSCEPTIBILITY TO, 1
166 0 1 2.4E-03 0 0
COLORECTAL CANCER, SUSCEPTIBILITY TO, 10
166 0 1 2.4E-03 0 0
COLORECTAL CANCER, SUSCEPTIBILITY TO, 12
166 0 1 2.4E-03 0 0
CUI: C1854494
Disease: Slow progression
Slow progression
165 0 1 2.4E-03 0 0
COLORECTAL CANCER, SUSCEPTIBILITY TO, 3
165 0 1 2.4E-03 0 0
CUI: C1837260
Disease: Prominent forehead
Prominent forehead
159 0 1 2.4E-03 0 0
CUI: C0917816
Disease: Mental deficiency
Mental deficiency
148 0 1 2.5E-03 0 0
CUI: C0018935
Disease: Hematocrit procedure
Hematocrit procedure
138 0 1 2.6E-03 0 0
CUI: C0152423
Disease: Congenital small ears
Congenital small ears
137 0 1 2.6E-03 0 0
Platelet Component Distribution Width Measurement
134 0 1 2.6E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color
130 0 1 2.6E-03 0 0
CUI: C1848673
Disease: Hypoplastic feet
Hypoplastic feet
129 0 1 2.6E-03 0 0
CUI: C0236969
Disease: Substance-Related Disorders
Substance-Related Disorders
128 0 1 2.6E-03 0 0
CUI: C0240543
Disease: Bulbous nose
Bulbous nose
123 0 1 2.7E-03 0 0
CUI: C0685409
Disease: Congenital Camptodactyly
Congenital Camptodactyly
123 0 1 2.7E-03 0 0
CUI: C0013222
Disease: Drug Use Disorders
Drug Use Disorders
121 0 1 2.7E-03 0 0
CUI: C1866934
Disease: Reduced tendon reflexes
Reduced tendon reflexes
121 0 1 2.7E-03 0 0
CUI: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly
120 0 1 2.7E-03 0 0