Congestive heart failure, and Left ventricular hypertrophy

Diseases related with Congestive heart failure and Left ventricular hypertrophy

In the following list you will find some of the most common rare diseases related to Congestive heart failure and Left ventricular hypertrophy that can help you solving undiagnosed cases.

Top matches:

Hereditary ventricular hypertrophy (CMH, HCM, ASH, or IHSS) in early stages produces a presystolic gallop due to an atrial heart sound, and EKG changes of ventricular hypertrophy. Progressive ventricular outflow obstruction may cause palpitation associated with arrhythmia, congestive heart failure, and sudden death. Seidman (2000) reviewed studies of hypertrophic cardiomyopathy in man and mouse. Genetic Heterogeneity of Hypertrophic CardiomyopathyAdditional forms of hypertrophic cardiomyopathy include CMH2 (OMIM ), caused by mutation in the TNNT2 gene (OMIM ) on chromosome 1q32; CMH3 (OMIM ), caused by mutation in the TPM1 gene (OMIM ) on chromosome 15q22; CMH4 (OMIM ), caused by mutation in the MYBPC3 gene (OMIM ) on chromosome 11p11; CMH6 (OMIM ), caused by mutation in the PRKAG2 gene (OMIM ) on chromosome 7q36; CMH7 (OMIM ), caused by mutation in the TNNI3 gene (OMIM ) on chromosome 19q13; CMH8 (OMIM ), caused by mutation in the MYL3 gene (OMIM ) on chromosome 3p21; CMH9 (see {188840}), caused by mutation in the TTN gene (OMIM ) on chromosome 2q31; CMH10 (see {160781}), caused by mutation in the MYL2 gene (OMIM ) on chromosome 12q24; CMH11 (OMIM ), caused by mutation in the ACTC1 gene (OMIM ) on chromosome 15q14; CMH12 (OMIM ), caused by mutation in the CSRP3 gene (OMIM ) on chromosome 11p15; CMH13 (OMIM ), caused by mutation in the TNNC1 gene (OMIM ) on chromosome 3p21; CMH14 (OMIM ), caused by mutation in the MYH6 gene (OMIM ) on chromosome 14q12; CMH15 (OMIM ), caused by mutation in the VCL gene (OMIM ) on chromosome 10q22; CMH16 (OMIM ), caused by mutation in the MYOZ2 gene (OMIM ) on chromosome 4q26; CMH17 (OMIM ), caused by mutation in the JPH2 gene (OMIM ) on chromosome 20q12; CMH18 (OMIM ), caused by mutation in the PLN gene (OMIM ) on chromosome 6q22; CMH19 (OMIM ), caused by mutation in the CALR3 gene (OMIM ) on chromosome 19p13; CMH20 (OMIM ), caused by mutation in the NEXN gene (OMIM ) on chromosome 1p31.1; CMH21, mapped to chromosome 7p12.1-q21; CMH22 (see {615248}), caused by mutation in the MYPN gene (OMIM ) on chromosome 10q21; CMH23 (see {612158}), caused by mutation in the ACTN2 gene (OMIM ) on chromosome 1q43; CMH24 (see {601493}), caused by mutation in the LDB3 gene (OMIM ) on chromosome 10q23; CMH25 (OMIM ), caused by mutation in the TCAP gene (OMIM ) on chromosome 17q12; CMH26 (OMIM ), caused by mutation in the FLNC gene (OMIM ) on chromosome 7q32; and CMH27 (OMIM ), caused by mutation in the ALPK3 gene (OMIM ) on chromosome 15q25.The CMH5 designation was initially assigned to a CMH family showing genetic heterogeneity. Subsequently, affected individuals were found to carry mutations in the MYH7 (CMH1) and/or MYBPC3 (CMH4) genes.Hypertrophic cardiomyopathy has also been associated with mutation in the gene encoding cardiac myosin light-peptide kinase (MYLK2; see {606566.0001}), which resides on chromosome 20q13.3; the gene encoding caveolin-3 (CAV3; see {601253.0013}), which maps to chromosome 3p25; and with mutations in genes encoding mitochondrial tRNAs: see mitochondrial tRNA-glycine (MTTG ) and mitochondrial tRNA-isoleucine (MTTI ).

CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1 Is also known as cmh|asymmetric septal hypertrophy|hypertrophic subaortic stenosis, idiopathic|ventricular hypertrophy, hereditary|ash

Related symptoms:

  • Cardiomyopathy
  • Congestive heart failure
  • Abnormality of metabolism/homeostasis
  • Arrhythmia
  • Hypertrophic cardiomyopathy


SOURCES: OMIM MENDELIAN

More info about CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1

Related symptoms:

  • Cardiomyopathy
  • Congestive heart failure
  • Dilated cardiomyopathy
  • Left ventricular hypertrophy
  • Ventricular tachycardia


SOURCES: MESH OMIM MENDELIAN

More info about CARDIOMYOPATHY, DILATED, 1P; CMD1P

Related symptoms:

  • Cardiomyopathy
  • Congestive heart failure
  • Dilated cardiomyopathy
  • Sudden cardiac death
  • Left ventricular hypertrophy


SOURCES: OMIM MESH MENDELIAN

More info about CARDIOMYOPATHY, DILATED, 1C, WITH OR WITHOUT LEFT VENTRICULAR NONCOMPACTION; CMD1C

Other less relevant matches:

Related symptoms:

  • Cardiomyopathy
  • Congestive heart failure
  • Dilated cardiomyopathy
  • Atrial fibrillation
  • Left ventricular hypertrophy


SOURCES: OMIM MENDELIAN

More info about CARDIOMYOPATHY, DILATED, 1HH; CMD1HH

Related symptoms:

  • Cardiomyopathy
  • Congestive heart failure
  • Hypertrophic cardiomyopathy
  • Tachycardia
  • Syncope


SOURCES: OMIM MENDELIAN

More info about CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 16; CMH16

Related symptoms:

  • Cardiomyopathy
  • Congestive heart failure
  • Hypertrophic cardiomyopathy
  • Dilated cardiomyopathy
  • Ventricular hypertrophy


SOURCES: OMIM MENDELIAN

More info about CARDIOMYOPATHY, DILATED, 1KK; CMD1KK

Related symptoms:

  • Respiratory distress
  • Cardiomyopathy
  • Congestive heart failure
  • Dyspnea
  • Hypertrophic cardiomyopathy


SOURCES: MESH OMIM MENDELIAN

More info about CARDIOMYOPATHY, DILATED, 1M; CMD1M

Related symptoms:

  • Hypertension
  • Cardiomyopathy
  • Congestive heart failure
  • Dyspnea
  • Hypertrophic cardiomyopathy


SOURCES: OMIM MENDELIAN

More info about CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 26; CMH26

Related symptoms:

  • Cardiomyopathy
  • Congestive heart failure
  • Arrhythmia
  • Dyspnea
  • Dilated cardiomyopathy


SOURCES: OMIM ORPHANET MENDELIAN

More info about FAMILIAL ATRIAL TACHYARRHYTHMIA-INFRA-HISIAN CARDIAC CONDUCTION DISEASE

Related symptoms:

  • Cardiomyopathy
  • Atrial septal defect
  • Congestive heart failure
  • Arrhythmia
  • Dyspnea


SOURCES: OMIM MESH MENDELIAN

More info about CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11; CMH11

Top 5 symptoms//phenotypes associated to Congestive heart failure and Left ventricular hypertrophy

Symptoms // Phenotype % cases
Cardiomyopathy Very Common - Between 80% and 100% cases
Dilated cardiomyopathy Common - Between 50% and 80% cases
Hypertrophic cardiomyopathy Common - Between 50% and 80% cases
Ventricular hypertrophy Common - Between 50% and 80% cases
Atrial fibrillation Common - Between 50% and 80% cases

Other less frequent symptoms

Patients with Congestive heart failure and Left ventricular hypertrophy. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases

Dyspnea Ventricular extrasystoles Left bundle branch block Bundle branch block Right bundle branch block Mitral regurgitation Arrhythmia

Rare Symptoms - Less than 30% cases

Tachycardia Reduced ejection fraction Sudden cardiac death Left ventricular noncompaction Ventricular arrhythmia Ventricular tachycardia Asymmetric septal hypertrophy Restrictive cardiomyopathy Atrioventricular block Supraventricular tachycardia Atrial flutter Paroxysmal atrial fibrillation Atrial arrhythmia Permanent atrial fibrillation Ventricular fibrillation Left anterior fascicular block Hypertension Multifocal atrial tachycardia Paroxysmal atrial tachycardia Atrial septal defect Myocardial infarction Cardiac arrest Heart block Left atrial enlargement Myocardial fibrosis Severely reduced ejection fraction Impaired myocardial contractility Abnormal left ventricle morphology Endocardial fibroelastosis Cardiomegaly Abnormality of metabolism/homeostasis Respiratory distress Moderately reduced ejection fraction Syncope First degree atrioventricular block Subvalvular aortic stenosis Muscular subvalvular aortic stenosis Endocardial fibrosis Wolff-Parkinson-White syndrome Reduced systolic function T-wave inversion


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