heart failure
Basic Information
- Identifier
- SYMP_0000292
- Notation
- SYMP:0000292
- Category
- symptoms
Related Diseases
- Alstrom syndrome
- Carney complex
- Cor pulmonale
- Holt-Oram syndrome
- Joubert syndrome 1
- Libman-Sacks endocarditis
- X-linked intellectual disability-cardiomegaly-congestive heart failure syndrome
- anomalous left coronary artery from the pulmonary artery
- atrial standstill 1
- atrial standstill 2
- autosomal dominant hypocalcemia 2
- cardiac arrest
- cardiac sarcoidosis
- cardiofaciocutaneous syndrome
- chorioangioma
- congenital dyserythropoietic anemia
- congenital nonspherocytic hemolytic anemia
- congestive heart failure
- dextro-looped transposition of the great arteries
- diastolic heart failure
- discrete subaortic stenosis
- fiedler's myocarditis
- generalized atherosclerosis
- heart conduction disease
- hemangioma of liver
- hemochromatosis type 2B
- hyperlipoproteinemia type IV
- infantile histiocytoid cardiomyopathy
- intravenous leiomyomatosis
- kyphoscoliotic heart disease
- mitochondrial DNA depletion syndrome 9
- mitochondrial pyruvate carrier deficiency
- mitral valve insufficiency
- mitral valve stenosis
- multiple mitochondrial dysfunctions syndrome 1
- nonbacterial thrombotic endocarditis
- obsolete Chagas cardiomyopathy
- obsolete Congenital cardiovascular disorder complicating pregnancy, childbirth, or the puerperium
- obsolete Coxiella burnetii pneumonia
- obsolete Toxoplasma myocarditis
- obsolete histoplasmosis endocarditis
- obsolete hydrops fetalis
- obsolete influenza myocarditis
- obsolete iron overload
- obsolete mitral valve syphilitic endocarditis
- obsolete primary Coxiellaceae infectious disease
- obsolete syphilitic endocarditis
- obsolete vesicoureteral reflux with reflux nephropathy
- pleural disease
- progressive familial heart block
- renal artery disease
- rheumatic congestive heart failure
- supravalvular aortic stenosis
- systolic heart failure
- transthyretin amyloidosis
- tricuspid atresia
- tricuspid valve insufficiency
- twin-to-twin transfusion syndrome
- uterus intravascular leiomyomatosis
- variant ABeta2M amyloidosis
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