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: C0311249
Disease: Cryptophthalmos
Cryptophthalmos 		1 0 1 5.0E-02 0 0
CUI: C1832931
Disease: ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 2 		1 0 1 5.0E-02 0 0
CUI: C1852453
Disease: Cryptophthalmos, Unilateral or Bilateral, Isolated
Cryptophthalmos, Unilateral or Bilateral, Isolated 		1 0 1 5.0E-02 0 0
CUI: C2315717
Disease: Cryptotia
Cryptotia 		1 0 1 5.0E-02 0 0
CUI: C2673198
Disease: Familial Cold Autoinflammatory Syndrome 2
Familial Cold Autoinflammatory Syndrome 2 		1 0 1 5.0E-02 0 0
CUI: C4014856
Disease: CONE-ROD DYSTROPHY 20
CONE-ROD DYSTROPHY 20 		1 0 1 5.0E-02 0 0
CUI: C4025329
Disease: Abnormality of the anus
Abnormality of the anus 		1 0 1 5.0E-02 0 0
CUI: C4053736
Disease: Catecholaminergic Polymorphic Ventricular Tachycardia Type 1
Catecholaminergic Polymorphic Ventricular Tachycardia Type 1 		1 0 1 5.0E-02 0 0
CUI: C4540036
Disease: FRASER SYNDROME 2
FRASER SYNDROME 2 		1 0 1 5.0E-02 0 0
CUI: C4551479
Disease: Schwartz-Jampel Syndrome, Type 1
Schwartz-Jampel Syndrome, Type 1 		1 0 1 5.0E-02 0 0
CUI: C0042510
Disease: Ventricular Fibrillation
Ventricular Fibrillation 		2 0 1 4.8E-02 0 0
CUI: C0085580
Disease: Essential Hypertension
Essential Hypertension 		2 0 1 4.8E-02 0 0
CUI: C0424448
Disease: Mask-like facies
Mask-like facies 		2 0 1 4.8E-02 0 0
CUI: C1849039
Disease: Metaphyseal widening
Metaphyseal widening 		2 0 1 4.8E-02 0 0
CUI: C1857453
Disease: Renal hypoplasia/aplasia
Renal hypoplasia/aplasia 		2 0 1 4.8E-02 0 0
CUI: C2677794
Disease: Stress-induced polymorphic ventricular tachycardia
Stress-induced polymorphic ventricular tachycardia 		2 0 1 4.8E-02 0 0
CUI: C0009714
Disease: Hepatic Fibrosis, Congenital
Hepatic Fibrosis, Congenital 		3 0 1 4.5E-02 0 0
CUI: C0340493
Disease: Paroxysmal familial ventricular fibrillation
Paroxysmal familial ventricular fibrillation 		3 0 1 4.5E-02 0 0
CUI: C0521622
Disease: Bilateral hydronephrosis
Bilateral hydronephrosis 		3 0 1 4.5E-02 0 0
CUI: C0152021
Disease: Congenital heart disease
Congenital heart disease 		5 0 1 4.2E-02 0 0
CUI: C0266294
Disease: Unilateral agenesis of kidney
Unilateral agenesis of kidney 		5 0 1 4.2E-02 0 0
CUI: C0266362
Disease: Ambiguous Genitalia
Ambiguous Genitalia 		5 0 1 4.2E-02 0 0
CUI: C1631597
Disease: VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder)
VENTRICULAR TACHYCARDIA, CATECHOLAMINERGIC POLYMORPHIC, 1 (disorder) 		5 0 1 4.2E-02 0 0
CUI: C0011981
Disease: Diaphragmatic Eventration
Diaphragmatic Eventration 		6 0 1 4.0E-02 0 0
CUI: C1858430
Disease: Death in infancy
Death in infancy 		6 0 1 4.0E-02 0 0