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: C0000737
Disease: Abdominal Pain
Abdominal Pain
9 11 1 4.5E-02 2 8.7E-02
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies
237 0 2 8.0E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior
13 0 1 3.8E-02 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia
17 0 1 3.3E-02 0 0
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly
9 24 1 4.5E-02 2 5.6E-02
CUI: C0003803
Disease: Arnold Chiari Malformation
Arnold Chiari Malformation
3 4 1 6.2E-02 2 0.12
CUI: C0003862
Disease: Arthralgia
Arthralgia
12 11 1 4.0E-02 2 8.7E-02
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis
16 25 1 3.4E-02 1 2.6E-02
CUI: C0004106
Disease: Astigmatism
Astigmatism
15 0 1 3.6E-02 0 0
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder
54 0 1 1.5E-02 0 0
CUI: C0004604
Disease: Back Pain
Back Pain
2 3 1 6.7E-02 2 0.13
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis
37 49 2 4.1E-02 1 1.6E-02
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia
44 0 1 1.8E-02 0 0
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
15 0 1 3.6E-02 0 0
CUI: C0008489
Disease: Chorea
Chorea
11 0 1 4.2E-02 0 0
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot
26 34 2 5.3E-02 1 2.1E-02
CUI: C0009806
Disease: Constipation
Constipation
40 49 3 5.9E-02 2 3.3E-02
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions
12 17 1 4.0E-02 1 3.3E-02
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism
35 0 2 4.3E-02 0 0
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
31 0 1 2.3E-02 0 0
CUI: C0011581
Disease: Depressive disorder
Depressive disorder
7 0 1 5.0E-02 0 0
CUI: C0011991
Disease: Diarrhea
Diarrhea
9 11 1 4.5E-02 2 8.7E-02
CUI: C0013132
Disease: Drooling
Drooling
14 0 2 7.7E-02 0 0
CUI: C0013274
Disease: Patent ductus arteriosus
Patent ductus arteriosus
23 25 1 2.8E-02 2 5.4E-02
CUI: C0013362
Disease: Dysarthria
Dysarthria
34 0 1 2.1E-02 0 0