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: C0003499
Disease: Supravalvular aortic stenosis
Supravalvular aortic stenosis
3 0 2 6.0E-03 0 0
CUI: C0003504
Disease: Aortic Valve Insufficiency
Aortic Valve Insufficiency
2 0 1 3.0E-03 0 0
CUI: C0003537
Disease: Aphasia
Aphasia
2 0 2 6.0E-03 0 0
CUI: C0003578
Disease: Apnea
Apnea
7 0 4 1.2E-02 0 0
CUI: C0003635
Disease: Apraxias
Apraxias
6 0 3 8.9E-03 0 0
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly
9 0 1 2.9E-03 0 0
CUI: C0003803
Disease: Arnold Chiari Malformation
Arnold Chiari Malformation
3 0 1 3.0E-03 0 0
CUI: C0003811
Disease: Cardiac Arrhythmia
Cardiac Arrhythmia
5 0 1 2.9E-03 0 0
CUI: C0003862
Disease: Arthralgia
Arthralgia
12 0 4 1.2E-02 0 0
CUI: C0003864
Disease: Arthritis
Arthritis
3 0 1 3.0E-03 0 0
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
6 0 1 2.9E-03 0 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis
16 25 4 1.2E-02 1 1.6E-03
CUI: C0004045
Disease: Asphyxia Neonatorum
Asphyxia Neonatorum
4 0 4 1.2E-02 0 0
CUI: C0004096
Disease: Asthma
Asthma
18 0 5 1.4E-02 0 0
CUI: C0004106
Disease: Astigmatism
Astigmatism
15 14 7 2.0E-02 2 3.2E-03
CUI: C0004114
Disease: Astrocytoma
Astrocytoma
5 0 3 8.9E-03 0 0
CUI: C0004134
Disease: Ataxia
Ataxia
14 0 4 1.2E-02 0 0
CUI: C0004138
Disease: Ataxias, Hereditary
Ataxias, Hereditary
1 0 1 3.0E-03 0 0
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
54 69 27 7.5E-02 3 4.4E-03
CUI: C0004779
Disease: Basal Cell Nevus Syndrome
Basal Cell Nevus Syndrome
3 0 1 3.0E-03 0 0
CUI: C0004903
Disease: Beckwith-Wiedemann Syndrome
Beckwith-Wiedemann Syndrome
3 0 1 3.0E-03 0 0
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome
5 0 1 2.9E-03 0 0
Malignant neoplasm of urinary bladder
7 17 1 2.9E-03 1 1.6E-03
CUI: C0005697
Disease: Neurogenic Urinary Bladder
Neurogenic Urinary Bladder
7 0 2 5.9E-03 0 0
CUI: C0005744
Disease: Blepharophimosis
Blepharophimosis
8 0 2 5.9E-03 0 0