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 11 3.3E-02 0 0
CUI: C0001125
Disease: Acidosis, Lactic
Acidosis, Lactic 		9 0 1 9.0E-03 0 0
CUI: C0001623
Disease: Adrenal gland hypofunction
Adrenal gland hypofunction 		2 2 1 9.6E-03 1 7.6E-03
CUI: C0002418
Disease: Amblyopia
Amblyopia 		17 0 2 1.7E-02 0 0
CUI: C0003467
Disease: Anxiety
Anxiety 		13 0 1 8.7E-03 0 0
CUI: C0003492
Disease: Aortic coarctation
Aortic coarctation 		3 0 1 9.5E-03 0 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		16 0 1 8.5E-03 0 0
CUI: C0004096
Disease: Asthma
Asthma 		18 0 1 8.3E-03 0 0
CUI: C0004138
Disease: Ataxias, Hereditary
Ataxias, Hereditary 		1 0 1 9.7E-03 0 0
CUI: C0004352
Disease: Autistic Disorder
Autistic Disorder 		54 0 2 1.3E-02 0 0
CUI: C0005586
Disease: Bipolar Disorder
Bipolar Disorder 		2 0 1 9.6E-03 0 0
CUI: C0005745
Disease: Blepharoptosis
Blepharoptosis 		37 0 1 7.2E-03 0 0
CUI: C0005754
Disease: Congenital blindness
Congenital blindness 		2 0 1 9.6E-03 0 0
CUI: C0006142
Disease: Malignant neoplasm of breast
Malignant neoplasm of breast 		28 802 1 7.7E-03 1 1.1E-03
CUI: C0006157
Disease: Breech Presentation
Breech Presentation 		10 0 1 8.9E-03 0 0
CUI: C0006267
Disease: Bronchiectasis
Bronchiectasis 		7 0 2 1.9E-02 0 0
CUI: C0007124
Disease: Noninfiltrating Intraductal Carcinoma
Noninfiltrating Intraductal Carcinoma 		5 4 1 9.3E-03 1 7.5E-03
CUI: C0007758
Disease: Cerebellar Ataxia
Cerebellar Ataxia 		44 0 4 2.8E-02 0 0
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		15 0 1 8.5E-03 0 0
CUI: C0007933
Disease: Meibomian Cyst
Meibomian Cyst 		2 0 1 9.6E-03 0 0
CUI: C0008297
Disease: Choanal Atresia
Choanal Atresia 		2 0 1 9.6E-03 0 0
CUI: C0008780
Disease: Ciliary Motility Disorders
Ciliary Motility Disorders 		36 0 1 7.2E-03 0 0
CUI: C0008924
Disease: Cleft upper lip
Cleft upper lip 		5 0 1 9.3E-03 0 0
CUI: C0009081
Disease: Congenital clubfoot
Congenital clubfoot 		26 0 2 1.6E-02 0 0
CUI: C0009363
Disease: Congenital ocular coloboma (disorder)
Congenital ocular coloboma (disorder) 		11 0 1 8.8E-03 0 0