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: C0002962
Disease: Angina Pectoris
Angina Pectoris 		2 0 1 2.3E-02 0 0
CUI: C0003886
Disease: Arthrogryposis
Arthrogryposis 		16 0 1 1.7E-02 0 0
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		2 0 1 2.3E-02 0 0
CUI: C0007789
Disease: Cerebral Palsy
Cerebral Palsy 		15 0 1 1.8E-02 0 0
CUI: C0009404
Disease: Colorectal Neoplasms
Colorectal Neoplasms 		31 0 1 1.4E-02 0 0
CUI: C0009691
Disease: Congenital cataract
Congenital cataract 		32 61 1 1.4E-02 1 2.0E-03
CUI: C0009806
Disease: Constipation
Constipation 		40 0 1 1.2E-02 0 0
CUI: C0010200
Disease: Coughing
Coughing 		6 0 1 2.1E-02 0 0
CUI: C0013132
Disease: Drooling
Drooling 		14 0 1 1.8E-02 0 0
CUI: C0013264
Disease: Muscular Dystrophy, Duchenne
Muscular Dystrophy, Duchenne 		1 0 1 2.3E-02 0 0
CUI: C0013274
Disease: Patent ductus arteriosus
Patent ductus arteriosus 		23 25 1 1.5E-02 1 2.1E-03
CUI: C0013481
Disease: Ebstein Anomaly
Ebstein Anomaly 		2 0 1 2.3E-02 0 0
CUI: C0013595
Disease: Eczema
Eczema 		15 0 1 1.8E-02 0 0
CUI: C0014877
Disease: Esotropia
Esotropia 		33 0 1 1.3E-02 0 0
CUI: C0015300
Disease: Exophthalmos
Exophthalmos 		7 0 1 2.0E-02 0 0
CUI: C0016842
Disease: Congenital pectus excavatum
Congenital pectus excavatum 		26 0 1 1.5E-02 0 0
CUI: C0017168
Disease: Gastroesophageal reflux disease
Gastroesophageal reflux disease 		2 0 1 2.3E-02 0 0
CUI: C0018794
Disease: Heart Block
Heart Block 		1 0 1 2.3E-02 0 0
CUI: C0018818
Disease: Ventricular Septal Defects
Ventricular Septal Defects 		31 0 1 1.4E-02 0 0
CUI: C0020224
Disease: Polyhydramnios
Polyhydramnios 		25 0 1 1.5E-02 0 0
CUI: C0020456
Disease: Hyperglycemia
Hyperglycemia 		10 0 1 1.9E-02 0 0
CUI: C0020490
Disease: Hyperopia
Hyperopia 		16 0 1 1.7E-02 0 0
CUI: C0020615
Disease: Hypoglycemia
Hypoglycemia 		12 15 1 1.9E-02 1 2.2E-03
CUI: C0021051
Disease: Immunologic Deficiency Syndromes
Immunologic Deficiency Syndromes 		9 0 1 2.0E-02 0 0
CUI: C0022387
Disease: Jervell-Lange Nielsen Syndrome
Jervell-Lange Nielsen Syndrome 		2 0 1 2.3E-02 0 0