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: C0021295
Disease: Infant, Premature, Diseases
Infant, Premature, Diseases
1 0 1 4.0E-02 0 0
Other specified hemorrhagic conditions
1 0 1 4.0E-02 0 0
CUI: C0029942
Disease: Overanxious disorder
Overanxious disorder
1 0 1 4.0E-02 0 0
CUI: C0178426
Disease: Oligohydramnios sequence
Oligohydramnios sequence
1 0 1 4.0E-02 0 0
CUI: C0240211
Disease: Lip swelling
Lip swelling
1 0 1 4.0E-02 0 0
CUI: C0263478
Disease: Ophiasis
Ophiasis
1 0 1 4.0E-02 0 0
CUI: C0334483
Disease: Adult rhabdomyoma
Adult rhabdomyoma
1 0 1 4.0E-02 0 0
CUI: C0340804
Disease: Hereditary vascular fragility
Hereditary vascular fragility
1 0 1 4.0E-02 0 0
CUI: C0342968
Disease: Impaired oxygen delivery
Impaired oxygen delivery
1 0 1 4.0E-02 0 0
CUI: C0345916
Disease: Neoplasm of ampulla of Vater
Neoplasm of ampulla of Vater
1 0 1 4.0E-02 0 0
CUI: C0520744
Disease: Paratracheal lymphadenopathy
Paratracheal lymphadenopathy
1 0 1 4.0E-02 0 0
CUI: C0585556
Disease: Macrosaccadic oscillations
Macrosaccadic oscillations
1 0 1 4.0E-02 0 0
CUI: C0685108
Disease: Lenegre's disease
Lenegre's disease
1 0 1 4.0E-02 0 0
CUI: C0747122
Disease: pacemaker ddd
pacemaker ddd
1 0 1 4.0E-02 0 0
CUI: C0748694
Disease: sick sinus
sick sinus
1 0 1 4.0E-02 0 0
CUI: C0751059
Disease: Cranial Neuropathies, Multiple
Cranial Neuropathies, Multiple
1 0 1 4.0E-02 0 0
CUI: C0795865
Disease: Chromosome 17, trisomy 17p
Chromosome 17, trisomy 17p
1 0 1 4.0E-02 0 0
CUI: C0854051
Disease: Allergy to sting
Allergy to sting
1 0 1 4.0E-02 0 0
CUI: C0857172
Disease: Persistent dry cough
Persistent dry cough
1 0 1 4.0E-02 0 0
CUI: C0877603
Disease: Anteroseptal infarction
Anteroseptal infarction
1 0 1 4.0E-02 0 0
CUI: C1142216
Disease: Epimacular membrane
Epimacular membrane
1 0 1 4.0E-02 0 0
CUI: C1168329
Disease: Flash pulmonary oedema
Flash pulmonary oedema
1 0 1 4.0E-02 0 0
CUI: C1265792
Disease: Chronic emphysema
Chronic emphysema
1 0 1 4.0E-02 0 0
Acute non-ST segment elevation myocardial infarction (disorder)
1 0 1 4.0E-02 0 0
CUI: C1695985
Disease: Lewis-Sumner syndrome
Lewis-Sumner syndrome
1 0 1 4.0E-02 0 0