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1.

Dilated cardiomyopathy

Dilated cardiomyopathy (DCM) is defined by the presence of left ventricular dilatation and left ventricular systolic dysfunction in the absence of abnormal loading conditions (hypertension, valve disease) or coronary artery disease sufficient to cause global systolic impairment. Right ventricular dilation and dysfunction may be present but are not necessary for the diagnosis. [from HPO]

MedGen UID:
504887
Concept ID:
CN001497
Finding
2.

Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome

Mental retardation, ovarian dysgenesis, congestive cardiomyopathy, broad nasal base, blepharoptosis, and bone abnormalities. The phenotype varies and not all features are present in individual cases. Occasional marfanoid habitus (tall stature with long and thin limbs, little subcutaneous fat, arachnodactyly, joint hyperextensibility, narrow face, small chin, large testes, and hypotonia). [from MCA/MR]

MedGen UID:
162901
Concept ID:
C0796031
Disease or Syndrome
3.

Nonischemic congestive cardiomyopathy

MedGen UID:
758723
Concept ID:
C3472699
Disease or Syndrome
4.

Secondary nonischemic congestive cardiomyopathy

MedGen UID:
784620
Concept ID:
C3697356
Disease or Syndrome
5.

Ischemic congestive cardiomyopathy

MedGen UID:
743625
Concept ID:
C1960867
Disease or Syndrome
6.

Dilated cardiomyopathy 1A

LMNA-related dilated cardiomyopathy (DCM) is caused by pathogenic variants in LMNA and is characterized by left ventricular enlargement and/or reduced systolic function preceded or accompanied by significant conduction system disease and/or arrhythmias. LMNA-related DCM usually presents in early to mid-adulthood with symptomatic conduction system disease or arrhythmias, or with symptomatic DCM including heart failure or embolus from a left ventricular mural thrombus. Sudden cardiac death can occur, and in some instances is the presenting manifestation; sudden cardiac death may occur with minimal or no systolic dysfunction. [from GTR]

MedGen UID:
258500
Concept ID:
C1449563
Disease or Syndrome
7.

Primary dilated cardiomyopathy

Nonsyndromic isolated dilated cardiomyopathy (DCM) is characterized by left ventricular enlargement and systolic dysfunction, a reduction in the myocardial force of contraction. DCM usually presents with any one of the following: Heart failure with symptoms of congestion (edema, orthopnea, paroxysmal nocturnal dyspnea) and/or reduced cardiac output (fatigue, dyspnea on exertion). Arrhythmias and/or conduction system disease. Thromboembolic disease (from left ventricular mural thrombus) including stroke. [from GTR]

MedGen UID:
2880
Concept ID:
C0007193
Disease or Syndrome
8.

Keshan disease

MedGen UID:
78639
Concept ID:
C0268095
Disease or Syndrome
9.

Fetal dilated cardiomyopathy

MedGen UID:
759364
Concept ID:
C3532251
Disease or Syndrome
10.

Ischemic dilated cardiomyopathy due to coronary artery disease

MedGen UID:
759345
Concept ID:
C3532232
Disease or Syndrome
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