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 		237 350 4 1.5E-02 1 2.4E-03
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		16 0 3 6.0E-02 0 0
CUI: C0004239
Disease: Atrial Flutter
Atrial Flutter 		2 2 2 5.4E-02 2 3.2E-02
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		54 69 2 2.2E-02 1 7.6E-03
CUI: C0005697
Disease: Neurogenic Urinary Bladder
Neurogenic Urinary Bladder 		7 0 1 2.3E-02 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		37 0 3 4.2E-02 0 0
CUI: C0006157
Disease: Breech Presentation
Breech Presentation 		10 0 1 2.2E-02 0 0
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		43 0 5 6.7E-02 0 0
CUI: C0007194
Disease: Hypertrophic Cardiomyopathy
Hypertrophic Cardiomyopathy 		29 468 2 3.1E-02 1 1.9E-03
CUI: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy 		6 0 1 2.4E-02 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		44 0 1 1.3E-02 0 0
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		15 19 1 2.0E-02 1 1.2E-02
CUI: C0007959
Disease: Charcot-Marie-Tooth Disease
Charcot-Marie-Tooth Disease 		24 0 3 5.2E-02 0 0
CUI: C0008031
Disease: Chest Pain
Chest Pain 		4 0 1 2.5E-02 0 0
CUI: C0008370
Disease: Cholestasis
Cholestasis 		4 0 1 2.5E-02 0 0
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		26 0 1 1.6E-02 0 0
CUI: C0009806
Disease: Constipation
Constipation 		40 0 3 4.1E-02 0 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		35 47 1 1.4E-02 1 9.2E-03
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders 		31 38 5 7.9E-02 4 4.1E-02
CUI: C0013132
Disease: Drooling
Drooling 		14 0 1 2.0E-02 0 0
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne 		1 0 1 2.7E-02 0 0
CUI: C0013362
Disease: Dysarthria
Dysarthria 		34 0 1 1.4E-02 0 0
CUI: C0013404
Disease: Dyspnea
Dyspnea 		18 21 4 7.8E-02 2 2.4E-02
CUI: C0013481
Disease: Ebstein Anomaly
Ebstein Anomaly 		2 0 1 2.6E-02 0 0
CUI: C0014877
Disease: Esotropia
Esotropia 		33 0 1 1.4E-02 0 0