MedGen for PMC (Select 4061768) - MedGen

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Links from PMC

Items: 5

Select item 2092321.

A myocardial disorder in which the heart muscle is structurally and functionally abnormal, in the absence of coronary artery disease, hypertension, valvular disease and congenital heart disease sufficient to cause the observed myocardial abnormality. [from HPO]

MedGen UID:: 209232
•Concept ID:: C0878544
•: Disease or Syndrome

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 7593522.

Cardiomyopathy, mitochondrial

MedGen UID:: 759352
•Concept ID:: C3532239
•: Disease or Syndrome

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 91693.

Congestive heart failure

The presence of an abnormality of cardiac function that is responsible for the failure of the heart to pump blood at a rate that is commensurate with the needs of the tissues or a state in which abnormally elevated filling pressures are required for the heart to do so. Heart failure is frequently related to a defect in myocardial contraction. [from HPO]

MedGen UID:: 9169
•Concept ID:: C0018802
•: Disease or Syndrome

GTR
ClinVar
Genes
OMIM
GeneReviews

Select item 67494.

Heart failure

Inability of the heart to pump blood at an adequate rate to meet tissue metabolic requirements. Clinical symptoms of heart failure include: unusual dyspnea on light exertion, recurrent dyspnea occurring in the supine position, fluid retention or rales, jugular venous distension, pulmonary edema on physical exam, or pulmonary edema on chest x-ray presumed to be cardiac dysfunction. [from NCI]