MYBPC3, myosin binding protein C3, 4607

N. diseases: 100; N. variants: 418
Source: ALL
Disease Type Disease Class Semantic Type N. genes d N. SNPs d Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
CUI: C3715165
Disease: LEFT VENTRICULAR NONCOMPACTION 10
LEFT VENTRICULAR NONCOMPACTION 10 		disease Disease or Syndrome 1 20 0.700 strong 1.000 9 20 1997 2019
CUI: C2751427
Disease: CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4, SUSCEPTIBILITY TO
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4, SUSCEPTIBILITY TO 		disease Finding 1 1 0.300 None 1.000 5 1 1999 2012
CUI: C3809346
Disease: CARDIOMYOPATHY, DILATED, 1MM
CARDIOMYOPATHY, DILATED, 1MM 		disease Disease or Syndrome 1 0.300 strong 1.000 2 2010 2017
CUI: C3665332
Disease: Primary hypertrophic cardiomyopathy
Primary hypertrophic cardiomyopathy 		disease Cardiovascular Diseases Disease or Syndrome 1 0.010 None 1.000 1 2006 2006
CUI: C1963282
Disease: Wolff-Parkinson-White Syndrome, CTCAE
Wolff-Parkinson-White Syndrome, CTCAE 		phenotype Finding 2 2 0.100 None 1.000 20 1 2006 2017
CUI: C1861862
Disease: Familial Hypertrophic Cardiomyopathy Type 4
Familial Hypertrophic Cardiomyopathy Type 4 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 3 145 0.900 definitive 1.000 118 143 1990 2019
CUI: C0750194
Disease: Non-sustained ventricular tachycardia
Non-sustained ventricular tachycardia 		disease Disease or Syndrome 5 0.010 None 1.000 1 2015 2015
CUI: C0597124
Disease: Obstructive asymmetric septal hypertrophy
Obstructive asymmetric septal hypertrophy 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 7 0.300 None 1.000 3 1997 2013
CUI: C0700053
Disease: Idiopathic hypertrophic subaortic stenosis
Idiopathic hypertrophic subaortic stenosis 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Congenital Abnormality 7 0.300 None 1.000 3 1997 2013
CUI: C0344955
Disease: Ventricular septal hypertrophy
Ventricular septal hypertrophy 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 8 3 0.100 None 0
CUI: C3495498
Disease: Cardiomyopathy, Familial Hypertrophic, 1 (disorder)
Cardiomyopathy, Familial Hypertrophic, 1 (disorder) 		disease Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 9 163 0.100 None 1.000 51 10 1990 2017
CUI: C2748884
Disease: CARDIOMYOPATHY, INFANTILE HYPERTROPHIC
CARDIOMYOPATHY, INFANTILE HYPERTROPHIC 		disease Disease or Syndrome 9 3 0.010 None 1.000 1 2008 2008
CUI: C4732796
Disease: Apical hypertrophic cardiomyopathy
Apical hypertrophic cardiomyopathy 		disease Cardiovascular Diseases Disease or Syndrome 10 3 0.010 None 1.000 1 2011 2011
CUI: C0281788
Disease: Biventricular hypertrophy
Biventricular hypertrophy 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 11 3 0.010 None 1.000 1 1 2012 2012
CUI: C0442887
Disease: Septal hypertrophy
Septal hypertrophy 		disease Acquired Abnormality 12 11 0.010 None 1.000 1 2012 2012
CUI: C1839832
Disease: Noncompaction cardiomyopathy
Noncompaction cardiomyopathy 		disease Cardiovascular Diseases Disease or Syndrome 17 5 0.110 None 1.000 1 1 2019 2019
CUI: C1861861
Disease: CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder)
CARDIOMYOPATHY, FAMILIAL RESTRICTIVE, 1 (disorder) 		disease Cardiovascular Diseases Disease or Syndrome 21 24 0.020 None 0.500 2 2015 2018
CUI: C0023211
Disease: Left Bundle-Branch Block
Left Bundle-Branch Block 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 25 1 0.100 None 0
CUI: C0233532
Disease: Maladaptive behavior associated with physical illness
Maladaptive behavior associated with physical illness 		phenotype Behavior and Behavior Mechanisms Mental or Behavioral Dysfunction 26 0.010 None 1.000 1 2019 2019
CUI: C0034063
Disease: Pulmonary Edema
Pulmonary Edema 		phenotype Respiratory Tract Diseases Pathologic Function 26 0.100 None 0
CUI: C1720824
Disease: Sudden Cardiac Arrest
Sudden Cardiac Arrest 		phenotype Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Pathologic Function 27 32 0.300 None 1.000 1 2010 2010
CUI: C0011071
Disease: Sudden death
Sudden death 		phenotype Pathological Conditions, Signs and Symptoms Pathologic Function 30 3 0.100 None 1.000 1 1 2016 2016
CUI: C0205700
Disease: Asymmetric Septal Hypertrophy
Asymmetric Septal Hypertrophy 		disease Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases Disease or Syndrome 31 7 0.110 None 1.000 1 1 2012 2012
CUI: C1960469
Disease: Left ventricular noncompaction
Left ventricular noncompaction 		disease Cardiovascular Diseases Disease or Syndrome 35 26 0.430 None 1.000 5 3 2009 2019
CUI: C0085615
Disease: Right bundle branch block
Right bundle branch block 		disease Pathological Conditions, Signs and Symptoms; Cardiovascular Diseases Disease or Syndrome 39 0.100 None 0