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
0 11 0 0 1 4.3E-02
CUI: C0002418
Disease: Amblyopia
Amblyopia
0 27 0 0 3 8.1E-02
CUI: C0003635
Disease: Apraxias
Apraxias
0 7 0 0 2 0.11
CUI: C0003706
Disease: Arachnodactyly
Arachnodactyly
0 24 0 0 1 2.8E-02
CUI: C0006157
Disease: Breech Presentation
Breech Presentation
0 11 0 0 1 4.3E-02
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy
0 19 0 0 2 6.7E-02
CUI: C0009806
Disease: Constipation
Constipation
0 49 0 0 1 1.6E-02
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions
0 24 0 0 1 2.8E-02
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders
0 39 0 0 2 4.0E-02
CUI: C0012569
Disease: Diplopia
Diplopia
0 5 0 0 2 0.12
CUI: C0013132
Disease: Drooling
Drooling
0 14 0 0 2 8.0E-02
CUI: C0013595
Disease: Eczema
Eczema
0 215 0 0 2 8.8E-03
CUI: C0014394
Disease: Enuresis
Enuresis
0 3 0 0 1 6.7E-02
CUI: C0014877
Disease: Esotropia
Esotropia
0 39 0 0 4 8.3E-02
CUI: C0015310
Disease: Exotropia
Exotropia
0 21 0 0 4 0.13
CUI: C0015732
Disease: Fecal Incontinence
Fecal Incontinence
0 12 0 0 1 4.2E-02
CUI: C0018681
Disease: Headache
Headache
0 51 0 0 1 1.6E-02
CUI: C0019572
Disease: Hirsutism
Hirsutism
0 17 0 0 1 3.4E-02
CUI: C0020295
Disease: Hydronephrosis
Hydronephrosis
0 17 0 0 1 3.4E-02
CUI: C0022602
Disease: Actinic keratosis
Actinic keratosis
0 2 0 0 2 0.15
CUI: C0023015
Disease: Language Disorders
Language Disorders
0 4 0 0 2 0.13
CUI: C0023221
Disease: Leg Length Inequality
Leg Length Inequality
0 6 0 0 2 0.12
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
0 240 0 0 2 8.0E-03
CUI: C0026827
Disease: Muscle hypotonia
Muscle hypotonia
0 579 0 0 4 6.8E-03
CUI: C0026837
Disease: Muscle Rigidity
Muscle Rigidity
0 10 0 0 2 9.5E-02