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: C0003119
Disease: Anophthalmos
Anophthalmos 		3 0 1 1.6E-02 0 0
CUI: C0003578
Disease: Apnea
Apnea 		7 0 1 1.5E-02 0 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		16 0 1 1.3E-02 0 0
CUI: C0004114
Disease: Astrocytoma
Astrocytoma 		5 0 1 1.5E-02 0 0
CUI: C0005744
Disease: Blepharophimosis
Blepharophimosis 		8 0 1 1.4E-02 0 0
CUI: C0005754
Disease: Congenital blindness
Congenital blindness 		2 0 1 1.6E-02 0 0
CUI: C0006118
Disease: Brain Neoplasms
Brain Neoplasms 		13 0 1 1.4E-02 0 0
CUI: C0007193
Disease: Cardiomyopathy, Dilated
Cardiomyopathy, Dilated 		43 0 1 9.6E-03 0 0
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		5 0 1 1.5E-02 0 0
CUI: C0009952
Disease: Febrile Convulsions
Febrile Convulsions 		12 0 1 1.4E-02 0 0
CUI: C0010038
Disease: Corneal Opacity
Corneal Opacity 		3 0 1 1.6E-02 0 0
CUI: C0010417
Disease: Cryptorchidism
Cryptorchidism 		35 0 1 1.0E-02 0 0
CUI: C0010495
Disease: Cutis Laxa
Cutis Laxa 		7 0 1 1.5E-02 0 0
CUI: C0011813
Disease: Dextrocardia
Dextrocardia 		6 0 1 1.5E-02 0 0
CUI: C0013363
Disease: Dysautonomia
Dysautonomia 		9 0 1 1.4E-02 0 0
CUI: C0014067
Disease: Occipital Encephalocele
Occipital Encephalocele 		6 0 3 4.6E-02 0 0
CUI: C0014544
Disease: Epilepsy
Epilepsy 		32 0 3 3.3E-02 0 0
CUI: C0014547
Disease: Epilepsies, Partial
Epilepsies, Partial 		8 0 2 2.9E-02 0 0
CUI: C0017601
Disease: Glaucoma
Glaucoma 		6 0 1 1.5E-02 0 0
CUI: C0017636
Disease: Glioblastoma
Glioblastoma 		22 0 1 1.2E-02 0 0
CUI: C0018817
Disease: Atrial Septal Defects
Atrial Septal Defects 		37 0 1 1.0E-02 0 0
CUI: C0020255
Disease: Hydrocephalus
Hydrocephalus 		22 0 1 1.2E-02 0 0
CUI: C0020505
Disease: Hyperphagia
Hyperphagia 		3 0 1 1.6E-02 0 0
CUI: C0020517
Disease: Hypersensitivity
Hypersensitivity 		1 0 1 1.6E-02 0 0
CUI: C0020619
Disease: Hypogonadism
Hypogonadism 		6 0 1 1.5E-02 0 0