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: C0000731
Disease: Abdomen distended
Abdomen distended
0 6 0 0 1 2.9E-02
CUI: C0002874
Disease: Aplastic Anemia
Aplastic Anemia
0 15 0 0 1 2.3E-02
CUI: C0004106
Disease: Astigmatism
Astigmatism
0 43 0 0 1 1.4E-02
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
0 49 0 0 1 1.3E-02
CUI: C0006157
Disease: Breech Presentation
Breech Presentation
0 11 0 0 1 2.5E-02
CUI: C0006267
Disease: Bronchiectasis
Bronchiectasis
0 8 0 0 1 2.7E-02
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy
0 470 0 0 1 2.0E-03
CUI: C0009806
Disease: Constipation
Constipation
0 49 0 0 1 1.3E-02
CUI: C0010278
Disease: Craniosynostosis
Craniosynostosis
0 33 0 0 1 1.6E-02
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
0 39 0 0 1 1.5E-02
CUI: C0013274
Disease: Patent ductus arteriosus
Patent ductus arteriosus
0 25 0 0 1 1.9E-02
CUI: C0013404
Disease: Dyspnea
Dyspnea
0 21 0 0 1 2.0E-02
CUI: C0015310
Disease: Exotropia
Exotropia
0 21 0 0 1 2.0E-02
CUI: C0015967
Disease: Fever
Fever
0 10 0 0 1 2.6E-02
CUI: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent
0 11 0 0 1 2.5E-02
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum
0 35 0 0 1 1.6E-02
CUI: C0017921
Disease: Glycogen storage disease type II
Glycogen storage disease type II
0 196 0 0 1 4.4E-03
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
0 43 0 0 1 1.4E-02
CUI: C0018916
Disease: Hemangioma
Hemangioma
0 15 0 0 1 2.3E-02
CUI: C0019270
Disease: Hernia
Hernia
0 1 0 0 1 3.3E-02
CUI: C0019322
Disease: Umbilical hernia
Umbilical hernia
0 17 0 0 1 2.2E-02
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios
0 28 0 0 1 1.8E-02
CUI: C0020534
Disease: Orbital separation excessive
Orbital separation excessive
0 77 0 0 1 9.4E-03
CUI: C0022346
Disease: Icterus
Icterus
0 10 0 0 1 2.6E-02
CUI: C0022595
Disease: Keratosis Follicularis
Keratosis Follicularis
0 20 0 0 2 4.2E-02