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: C0030215
Disease: Palatal Neoplasms
Palatal Neoplasms
0 2 0 0 1 1.1E-02
CUI: C0035085
Disease: Renal infarction
Renal infarction
0 1 0 0 1 1.1E-02
Infections specific to perinatal period
0 1 0 0 1 1.1E-02
CUI: C0242453
Disease: Prostatism
Prostatism
0 1 0 0 1 1.1E-02
CUI: C0265329
Disease: Organoid Nevus Phakomatosis
Organoid Nevus Phakomatosis
0 9 0 0 1 1.0E-02
CUI: C0268275
Disease: Tay-Sachs Disease, AB Variant
Tay-Sachs Disease, AB Variant
0 7 0 0 1 1.0E-02
Non-small cell lung cancer stage III
0 1 0 0 1 1.1E-02
CUI: C0334279
Disease: Adenocarcinoma, intestinal type
Adenocarcinoma, intestinal type
0 2 0 0 1 1.1E-02
CUI: C0796003
Disease: Juberg-Marsidi syndrome
Juberg-Marsidi syndrome
0 14 0 0 1 9.7E-03
CUI: C0948698
Disease: Coronary spastic angina
Coronary spastic angina
0 1 0 0 1 1.1E-02
HYPERTENSION, RESISTANT TO CONVENTIONAL THERAPY
0 1 0 0 1 1.1E-02
CUI: C3495893
Disease: Congenital thrombophilia
Congenital thrombophilia
0 1 0 0 1 1.1E-02
CUI: C3540839
Disease: Neonatal Drug Withdrawal
Neonatal Drug Withdrawal
0 3 0 0 1 1.1E-02
Homozygous methylenetetrahydrofolate reductase mutation
0 1 0 0 1 1.1E-02
Primary low grade serous adenocarcinoma of ovary
0 1 0 0 1 1.1E-02
CUI: C4511035
Disease: Isolated thrombocytopenia
Isolated thrombocytopenia
0 9 0 0 1 1.0E-02
CUI: C0028077
Disease: Nyctalopia
Nyctalopia
168 0 1 2.1E-03 0 0
CUI: C1836038
Disease: Poor head control
Poor head control
162 0 1 2.2E-03 0 0
CUI: C0038271
Disease: Stereotyped Behavior
Stereotyped Behavior
135 0 1 2.3E-03 0 0
CUI: C0476403
Disease: Electromyogram abnormal
Electromyogram abnormal
130 0 1 2.3E-03 0 0
CUI: C4025846
Disease: Abnormality of vision
Abnormality of vision
127 0 1 2.4E-03 0 0
CUI: C1866195
Disease: Downturned corners of mouth
Downturned corners of mouth
122 0 1 2.4E-03 0 0
CUI: C0424574
Disease: Duration of sleep
Duration of sleep
104 0 1 2.5E-03 0 0
CUI: C0270922
Disease: Peripheral demyelinating neuropathy
Peripheral demyelinating neuropathy
95 0 1 2.5E-03 0 0
CUI: C0009398
Disease: Color vision defect
Color vision defect
94 0 1 2.6E-03 0 0