Congestive heart failure, and Ventricular hypertrophy

Diseases related with Congestive heart failure and Ventricular hypertrophy

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

Top matches:

Familial glucocorticoid deficiency-5 is characterized by resistance to adrenocorticotropic hormone (ACTH) and isolated glucocorticoid deficiency, with typical biochemical findings of low serum cortisol levels and high plasma ACTH. Patients commonly present with hyperpigmentation (Prasad et al., 2014).For a discussion of genetic heterogeneity of familial glucocorticoid deficiency, see GCCD1 (OMIM ).

Related symptoms:

  • Ventricular septal defect
  • Congestive heart failure
  • Truncus arteriosus


SOURCES: OMIM MENDELIAN

More info about GLUCOCORTICOID DEFICIENCY 5; GCCD5

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

Other less relevant matches:

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

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

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

Symptoms // Phenotype % cases
Cardiomyopathy Very Common - Between 80% and 100% cases
Left ventricular hypertrophy Very Common - Between 80% and 100% cases
Dilated cardiomyopathy Common - Between 50% and 80% cases
Atrial fibrillation Uncommon - Between 30% and 50% cases
Hypertrophic cardiomyopathy Uncommon - Between 30% and 50% cases

Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases

Left bundle branch block Right bundle branch block Ventricular extrasystoles Bundle branch block Dyspnea

Rare Symptoms - Less than 30% cases

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


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