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: C0340427
Disease: Familial dilated cardiomyopathy
Familial dilated cardiomyopathy 		10 32 4 0.31 2 1.6E-02
CUI: C0149721
Disease: Left Ventricular Hypertrophy
Left Ventricular Hypertrophy 		5 0 2 0.20 0 0
CUI: C0007196
Disease: Restrictive cardiomyopathy
Restrictive cardiomyopathy 		6 15 2 0.18 1 9.3E-03
CUI: C0043202
Disease: Wolff-Parkinson-White Syndrome
Wolff-Parkinson-White Syndrome 		14 16 3 0.17 2 1.9E-02
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		8 19 2 0.15 1 9.0E-03
CUI: C0949658
Disease: Cardiomyopathy, Hypertrophic, Familial
Cardiomyopathy, Hypertrophic, Familial 		24 332 4 0.15 48 0.13
CUI: C0018794
Disease: Heart Block
Heart Block 		1 0 1 0.14 0 0
CUI: C0205700
Disease: Asymmetric Septal Hypertrophy
Asymmetric Septal Hypertrophy 		1 0 1 0.14 0 0
CUI: C0221347
Disease: Acrocyanosis
Acrocyanosis 		1 0 1 0.14 0 0
CUI: C0264886
Disease: Conduction disorder of the heart
Conduction disorder of the heart 		1 0 1 0.14 0 0
CUI: C0270960
Disease: Congenital myopathy (disorder)
Congenital myopathy (disorder) 		1 0 1 0.14 0 0
CUI: C1832243
Disease: CARDIOMYOPATHY, DILATED, 1D (disorder)
CARDIOMYOPATHY, DILATED, 1D (disorder) 		1 24 1 0.14 1 8.6E-03
CUI: C1832916
Disease: Timothy syndrome
Timothy syndrome 		1 0 1 0.14 0 0
CUI: C1834696
Disease: Hyporeflexia of lower limbs
Hyporeflexia of lower limbs 		1 0 1 0.14 0 0
CUI: C1836835
Disease: Hyporeflexia of upper limbs
Hyporeflexia of upper limbs 		1 0 1 0.14 0 0
CUI: C1837471
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 8 		1 6 1 0.14 1 1.0E-02
CUI: C1837650
Disease: Lack of spontaneous play
Lack of spontaneous play 		1 0 1 0.14 0 0
CUI: C1842160
Disease: MYOPATHY, MYOSIN STORAGE (disorder)
MYOPATHY, MYOSIN STORAGE (disorder) 		1 14 1 0.14 12 0.13
CUI: C1850709
Disease: Myopathy, Hyaline Body, Autosomal Recessive
Myopathy, Hyaline Body, Autosomal Recessive 		1 11 1 0.14 10 0.11
CUI: C1856477
Disease: Slowed horizontal saccades
Slowed horizontal saccades 		1 0 1 0.14 0 0
CUI: C1861864
Disease: Cardiomyopathy, Familial Hypertrophic, 2
Cardiomyopathy, Familial Hypertrophic, 2 		1 26 1 0.14 1 8.5E-03
CUI: C2676271
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 3 (disorder) 		1 21 1 0.14 1 8.8E-03
CUI: C2678478
Disease: Brugada Syndrome 3
Brugada Syndrome 3 		1 0 1 0.14 0 0
CUI: C2750466
Disease: Cardiomyopathy, Dilated, 1EE
Cardiomyopathy, Dilated, 1EE 		1 0 1 0.14 0 0
CUI: C2750467
Disease: Cardiomyopathy, Familial Hypertrophic, 14
Cardiomyopathy, Familial Hypertrophic, 14 		1 0 1 0.14 0 0