Congestive heart failure, and Atrial septal defect

Diseases related with Congestive heart failure and Atrial septal defect

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


Top matches:

Medium match GLUCOCORTICOID DEFICIENCY 5; GCCD5


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

Medium match VENTRICULAR SEPTAL DEFECT 1; VSD1


Ventricular septal defect (VSD) is the most common form of congenital cardiovascular anomaly, occurring in nearly 50% of all infants with a congenital heart defect and accounting for 14 to 16% of cardiac defects that require invasive treatment within the first year of life. Congenital VSDs may occur alone or in combination with other cardiac malformations. Large VSDs that go unrepaired may give rise to cardiac enlargement, congestive heart failure, pulmonary hypertension, Eisenmenger's syndrome, delayed fetal brain development, arrhythmias, and even sudden cardiac death (summary by {3,4:Wang et al., 2011, 2011}).Other congenital cardiac defects caused by mutation in the GATA4 gene include atrial septal defect (ASD2 ), tetralogy of Fallot (see TOF, {187500}), and endocardial cushion defects (AVSD4 ). Genetic Heterogeneity of Ventricular Septal DefectVSD2 (OMIM ) is caused by mutation in the CITED2 gene (OMIM ) on chromosome 6q24; VSD3 (OMIM ) is caused by mutation in the NKX2-5 gene (OMIM ) on chromosome 5q34.Somatic mutations in the HAND1 gene (OMIM ) have been identified in tissue samples from patients with VSD.

Related symptoms:

  • Hypertension
  • Ventricular septal defect
  • Atrial septal defect
  • Congestive heart failure
  • Abnormality of cardiovascular system morphology


SOURCES: OMIM MENDELIAN

More info about VENTRICULAR SEPTAL DEFECT 1; VSD1

Medium match CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11; CMH11


Related symptoms:

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


SOURCES: OMIM MESH MENDELIAN

More info about CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 11; CMH11

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Other less relevant matches:

Medium match CARDIOMYOPATHY, DILATED, 1R; CMD1R


Related symptoms:

  • Ventricular septal defect
  • Cardiomyopathy
  • Atrial septal defect
  • Congestive heart failure
  • Hypertrophic cardiomyopathy


SOURCES: OMIM MENDELIAN

More info about CARDIOMYOPATHY, DILATED, 1R; CMD1R

Medium match VENTRICULAR SEPTAL DEFECT 3; VSD3


Ventricular septal defect (VSD) is the most common form of congenital cardiovascular anomaly, occurring in nearly 50% of all infants with a congenital heart defect and accounting for 14 to 16% of cardiac defects that require invasive treatment within the first year of life. Congenital VSDs may occur alone or in combination with other cardiac malformations. Large VSDs that go unrepaired may give rise to cardiac enlargement, congestive heart failure, pulmonary hypertension, Eisenmenger's syndrome, delayed fetal brain development, arrhythmias, and even sudden cardiac death (summary by {3,4:Wang et al., 2011, 2011}).Other congenital cardiac defects caused by mutation in the NKX2-5 gene include atrial septal defect with or without atrioventricular conduction defects (ASD7 ), tetralogy of Fallot (see TOF, {187500}), conotruncal malformations (see {217095}), and hypoplastic left heart syndrome (HLHS2 ).For a discussion of genetic heterogeneity of ventricular septal defect, see VSD1 (OMIM ).

Related symptoms:

  • Hypertension
  • Ventricular septal defect
  • Atrial septal defect
  • Congestive heart failure
  • Abnormality of cardiovascular system morphology


SOURCES: OMIM MENDELIAN

More info about VENTRICULAR SEPTAL DEFECT 3; VSD3

Medium match ATRIOVENTRICULAR SEPTAL DEFECT 3; AVSD3


Related symptoms:

  • Hypertension
  • Congestive heart failure
  • Cyanosis
  • Pulmonary arterial hypertension
  • First degree atrioventricular block


SOURCES: OMIM MENDELIAN

More info about ATRIOVENTRICULAR SEPTAL DEFECT 3; AVSD3

Medium match CARDIOMYOPATHY, DILATED, 1Y; CMD1Y


Related symptoms:

  • Pain
  • Respiratory distress
  • Cardiomyopathy
  • Edema
  • Atrial septal defect


SOURCES: OMIM MESH MENDELIAN

More info about CARDIOMYOPATHY, DILATED, 1Y; CMD1Y

Medium match ATRIAL SEPTAL DEFECT 4; ASD4


Related symptoms:

  • Hypertension
  • Ventricular septal defect
  • Cardiomyopathy
  • Atrial septal defect
  • Congestive heart failure


SOURCES: OMIM MESH MENDELIAN

More info about ATRIAL SEPTAL DEFECT 4; ASD4

Medium match CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2


Related symptoms:

  • Ventricular septal defect
  • Edema
  • Atrial septal defect
  • Congestive heart failure
  • Abnormal heart morphology


SOURCES: OMIM MENDELIAN

More info about CONGENITAL HEART DEFECTS, MULTIPLE TYPES, 2; CHTD2

Top 5 symptoms//phenotypes associated to Congestive heart failure and Atrial septal defect

Symptoms // Phenotype % cases
Ventricular septal defect Common - Between 50% and 80% cases
Sudden cardiac death Uncommon - Between 30% and 50% cases
Atrial fibrillation Uncommon - Between 30% and 50% cases
Dilated cardiomyopathy Uncommon - Between 30% and 50% cases
Cardiomyopathy Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Congestive heart failure and Atrial septal defect. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Abnormal heart morphology Arrhythmia Hypertrophic cardiomyopathy Hypertension Pulmonary arterial hypertension Dyspnea Left ventricular noncompaction Left ventricular hypertrophy Myocarditis

Rare Symptoms - Less than 30% cases


Ventricular tachycardia Left ventricular noncompaction cardiomyopathy Tachycardia Endocardial fibroelastosis Ventricular arrhythmia Edema Syncope Myocardial infarction Cardiac arrest Mitral regurgitation Abnormality of cardiovascular system morphology Ventricular hypertrophy Pulmonary artery atresia Subvalvular aortic stenosis Myxomatous mitral valve degeneration Dilatation Atrioventricular block Ventricular fibrillation Bundle branch block Esophageal atresia Abnormal EKG Right ventricular hypertrophy Left bundle branch block Bicuspid aortic valve Supraventricular tachycardia Reduced ejection fraction Secundum atrial septal defect Myocardial fibrosis Asymmetric septal hypertrophy Left ventricular failure Supraventricular arrhythmia Biventricular hypertrophy Endocardial fibrosis Premature atrial contractions Cardiomyocyte hypertrophy Aortic aneurysm Tetralogy of Fallot Aortic regurgitation Inlet ventricular septal defect Heart block Restrictive cardiomyopathy ST segment depression Patent ductus arteriosus Hypoplastic left heart Pulmonary artery stenosis Cyanosis First degree atrioventricular block Primum atrial septal defect Midsystolic murmur Pain Aortic valve stenosis Respiratory distress Chest pain Palpitations Pulmonic stenosis Mitral valve prolapse Coarctation of aorta Patent foramen ovale Mitral stenosis Truncus arteriosus T-wave inversion Hydrops fetalis Myofiber disarray



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