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: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele
0 9 0 0 1 1.9E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 2.2E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant
0 7 0 0 1 2.0E-02
Acute idiopathic thrombocytopenic purpura
0 1 0 0 1 2.2E-02
CUI: C0741585
Disease: BODY ACHE
BODY ACHE
0 1 0 0 1 2.2E-02
CUI: C3266076
Disease: Orofacial cleft
Orofacial cleft
0 2 0 0 2 4.4E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 2.1E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 2.2E-02
CUI: C4733577
Disease: adult chronic myelogenous leukemia
adult chronic myelogenous leukemia
0 3 0 0 3 6.7E-02
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
208 0 1 2.2E-03 0 0
CUI: C2267233
Disease: Neonatal Hypotonia
Neonatal Hypotonia
169 0 1 2.4E-03 0 0
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 1 2.4E-03 0 0
CUI: C0038580
Disease: Substance Dependence
Substance Dependence
156 0 1 2.5E-03 0 0
CUI: C1853743
Disease: Muscular hypotonia of the trunk
Muscular hypotonia of the trunk
156 0 1 2.5E-03 0 0
CUI: C0020490
Disease: Hyperopia
Hyperopia
142 0 1 2.6E-03 0 0
CUI: C0018498
Disease: Hair Color
Hair Color
130 0 1 2.7E-03 0 0
Congenital ocular coloboma (disorder)
129 0 1 2.7E-03 0 0
CUI: C0266483
Disease: Pachygyria
Pachygyria
129 0 1 2.7E-03 0 0
CUI: C0266544
Disease: Microcornea
Microcornea
129 0 1 2.7E-03 0 0
CUI: C0236969
Disease: Substance-Related Disorders
Substance-Related Disorders
128 0 1 2.7E-03 0 0
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision
127 0 1 2.7E-03 0 0
CUI: C0685409
Disease: Congenital Camptodactyly
Congenital Camptodactyly
123 0 1 2.7E-03 0 0
CUI: C1866195
Disease: Downturned corners of mouth
Downturned corners of mouth
122 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: C0221369
Disease: Acquired Camptodactyly
Acquired Camptodactyly
120 0 1 2.7E-03 0 0