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: C0000731
Disease: Abdomen distended
Abdomen distended 		6 0 1 8.3E-02 0 0
CUI: C0000772
Disease: Multiple congenital anomalies
Multiple congenital anomalies 		237 0 1 4.1E-03 0 0
CUI: C0003862
Disease: Arthralgia
Arthralgia 		12 0 1 5.6E-02 0 0
CUI: C0004106
Disease: Astigmatism
Astigmatism 		15 0 1 4.8E-02 0 0
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		54 0 1 1.7E-02 0 0
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		44 0 2 4.1E-02 0 0
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions 		12 0 1 5.6E-02 0 0
CUI: C0011168
Disease: Deglutition Disorders
Deglutition Disorders 		31 0 1 2.7E-02 0 0
CUI: C0011813
Disease: Dextrocardia
Dextrocardia 		6 0 1 8.3E-02 0 0
CUI: C0013404
Disease: Dyspnea
Dyspnea 		18 0 1 4.2E-02 0 0
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		6 0 1 8.3E-02 0 0
CUI: C0014544
Disease: Epilepsy
Epilepsy 		32 0 1 2.6E-02 0 0
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial 		8 0 1 7.1E-02 0 0
CUI: C0014877
Disease: Esotropia
Esotropia 		33 0 1 2.6E-02 0 0
CUI: C0018681
Disease: Headache
Headache 		19 0 1 4.0E-02 0 0
CUI: C0022595
Disease: Keratosis Follicularis
Keratosis Follicularis 		13 0 1 5.3E-02 0 0
CUI: C0022680
Disease: Polycystic Kidney Diseases
Polycystic Kidney Diseases 		21 0 1 3.7E-02 0 0
CUI: C0025362
Disease: Mental Retardation
Mental Retardation 		28 0 1 2.9E-02 0 0
CUI: C0027092
Disease: Myopia
Myopia 		45 0 1 2.0E-02 0 0
CUI: C0028738
Disease: Nystagmus
Nystagmus 		62 0 1 1.5E-02 0 0
CUI: C0029453
Disease: Osteopenia
Osteopenia 		23 0 1 3.4E-02 0 0
CUI: C0031039
Disease: Pericardial effusion
Pericardial effusion 		6 0 1 8.3E-02 0 0
CUI: C0036341
Disease: Schizophrenia
Schizophrenia 		6 0 1 8.3E-02 0 0
CUI: C0036439
Disease: Scoliosis, unspecified
Scoliosis, unspecified 		63 0 1 1.4E-02 0 0
CUI: C0038379
Disease: Strabismus
Strabismus 		61 0 1 1.5E-02 0 0