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
237 350 1 3.7E-03 3 4.0E-03
CUI: C0004096
Disease: Asthma
Asthma
18 19 1 1.9E-02 2 4.8E-03
CUI: C0004099
Disease: Asthma, Exercise-Induced
Asthma, Exercise-Induced
1 2 1 2.8E-02 2 5.0E-03
CUI: C0004144
Disease: Atelectasis
Atelectasis
1 2 1 2.8E-02 2 5.0E-03
CUI: C0006267
Disease: Bronchiectasis
Bronchiectasis
7 8 2 4.9E-02 2 4.9E-03
CUI: C0008031
Disease: Chest Pain
Chest Pain
4 5 1 2.6E-02 2 4.9E-03
CUI: C0010200
Disease: Coughing
Coughing
6 7 2 5.0E-02 2 4.9E-03
CUI: C0013404
Disease: Dyspnea
Dyspnea
18 21 2 3.8E-02 2 4.8E-03
CUI: C0014591
Disease: Epistaxis
Epistaxis
3 4 1 2.6E-02 2 5.0E-03
CUI: C0016202
Disease: Flatfoot
Flatfoot
30 38 1 1.5E-02 1 2.3E-03
CUI: C0018536
Disease: Hallux Valgus
Hallux Valgus
5 0 1 2.5E-02 0 0
CUI: C0018681
Disease: Headache
Headache
19 23 1 1.9E-02 2 4.7E-03
CUI: C0022680
Disease: Polycystic Kidney Diseases
Polycystic Kidney Diseases
21 0 1 1.8E-02 0 0
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
162 0 1 5.1E-03 0 0
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
336 579 2 5.4E-03 1 1.0E-03
CUI: C0032227
Disease: Pleural effusion disorder
Pleural effusion disorder
8 11 1 2.3E-02 2 4.9E-03
CUI: C0032231
Disease: Pleurisy
Pleurisy
1 2 1 2.8E-02 2 5.0E-03
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa
88 0 1 8.1E-03 0 0
CUI: C0035455
Disease: Rhinitis
Rhinitis
1 2 1 2.8E-02 2 5.0E-03
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified
63 92 1 1.0E-02 2 4.1E-03
CUI: C0036572
Disease: Seizures
Seizures
237 0 1 3.7E-03 0 0
CUI: C0037221
Disease: Situs Inversus
Situs Inversus
4 3 1 2.6E-02 1 2.5E-03
CUI: C0039070
Disease: Syncope
Syncope
8 12 1 2.3E-02 2 4.9E-03
CUI: C0039075
Disease: Syndactyly
Syndactyly
13 0 1 2.1E-02 0 0
CUI: C0040264
Disease: Tinnitus
Tinnitus
6 7 1 2.4E-02 2 4.9E-03