Source: CLINVAR ×
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 0 1 4.1E-03 0 0
CUI: C0001807
Disease: Aggressive behavior
Aggressive behavior 		13 0 1 4.5E-02 0 0
CUI: C0002418
Disease: Amblyopia
Amblyopia 		17 0 1 3.8E-02 0 0
CUI: C0003079
Disease: Anisocoria
Anisocoria 		4 5 1 7.7E-02 1 5.6E-02
CUI: C0003862
Disease: Arthralgia
Arthralgia 		12 11 1 4.8E-02 1 4.2E-02
CUI: C0004096
Disease: Asthma
Asthma 		18 19 1 3.7E-02 1 3.1E-02
CUI: C0004106
Disease: Astigmatism
Astigmatism 		15 0 1 4.2E-02 0 0
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		54 69 1 1.6E-02 1 1.2E-02
CUI: C0008489
Disease: Chorea
Chorea 		11 0 1 5.0E-02 0 0
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions 		12 0 1 4.8E-02 0 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		35 0 1 2.3E-02 0 0
CUI: C0011334
Disease: Dental caries
Dental caries 		7 7 1 6.2E-02 1 5.0E-02
CUI: C0011581
Disease: Depressive disorder
Depressive disorder 		7 0 1 6.2E-02 0 0
CUI: C0013363
Disease: Dysautonomia
Dysautonomia 		9 0 1 5.6E-02 0 0
CUI: C0014390
Disease: Entropion
Entropion 		1 1 1 1.0E-01 1 7.1E-02
CUI: C0014877
Disease: Esotropia
Esotropia 		33 0 1 2.4E-02 0 0
CUI: C0015732
Disease: Fecal Incontinence
Fecal Incontinence 		10 12 1 5.3E-02 1 4.0E-02
CUI: C0016202
Disease: Flatfoot
Flatfoot 		30 0 1 2.6E-02 0 0
CUI: C0017639
Disease: Gliosis
Gliosis 		4 3 1 7.7E-02 1 6.2E-02
CUI: C0018681
Disease: Headache
Headache 		19 23 1 3.6E-02 1 2.8E-02
CUI: C0018777
Disease: Conductive hearing loss
Conductive hearing loss 		3 0 1 8.3E-02 0 0
CUI: C0018916
Disease: Hemangioma
Hemangioma 		12 0 1 4.8E-02 0 0
CUI: C0019294
Disease: Hernia, Inguinal
Hernia, Inguinal 		13 15 1 4.5E-02 1 3.6E-02
CUI: C0019322
Disease: Umbilical hernia
Umbilical hernia 		17 17 1 3.8E-02 1 3.3E-02
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios 		25 28 1 2.9E-02 1 2.4E-02