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: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
0 350 0 0 1 2.7E-03
CUI: C0002874
Disease: Aplastic Anemia
Aplastic Anemia
0 15 0 0 1 3.0E-02
CUI: C0003635
Disease: Apraxias
Apraxias
0 7 0 0 1 4.0E-02
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly
0 24 0 0 1 2.4E-02
CUI: C0004045
Disease: Asphyxia Neonatorum
Asphyxia Neonatorum
0 4 0 0 2 9.5E-02
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
0 181 0 0 4 2.0E-02
CUI: C0005744
Disease: Blepharophimosis
Blepharophimosis
0 15 0 0 1 3.0E-02
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy
0 470 0 0 1 2.0E-03
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot
0 35 0 0 4 8.0E-02
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms
0 586 0 0 1 1.7E-03
CUI: C0010308
Disease: Congenital Hypothyroidism
Congenital Hypothyroidism
0 9 0 0 1 3.7E-02
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
0 48 0 0 1 1.5E-02
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
0 39 0 0 1 1.8E-02
CUI: C0011334
Disease: Dental caries
Dental caries
0 72 0 0 1 1.1E-02
CUI: C0014877
Disease: Esotropia
Esotropia
0 39 0 0 1 1.8E-02
CUI: C0015230
Disease: Exanthema
Exanthema
0 3 0 0 2 1.0E-01
CUI: C0015300
Disease: Exophthalmos
Exophthalmos
0 10 0 0 1 3.6E-02
CUI: C0016202
Disease: Flatfoot
Flatfoot
0 38 0 0 2 3.6E-02
CUI: C0016522
Disease: Foramen Ovale, Patent
Foramen Ovale, Patent
0 11 0 0 1 3.4E-02
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum
0 35 0 0 1 1.9E-02
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease
0 31 0 0 1 2.0E-02
Sensorineural Hearing Loss (disorder)
0 44 0 0 1 1.6E-02
CUI: C0018808
Disease: Heart murmur
Heart murmur
0 10 0 0 2 7.4E-02
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects
0 43 0 0 2 3.3E-02
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects
0 34 0 0 1 1.9E-02