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Human Phenotype Ontology
Last uploaded:
August 13, 2024
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| Preferred Name | Dilated cardiomyopathy | |
| Synonyms |
Stretched and thinned heart muscle Cardiomyopathy, dilated DCM Congestive cardiomyopathy |
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| Definitions |
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. |
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| ID |
http://purl.obolibrary.org/obo/HP_0001644 |
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| database_cross_reference |
Fyler:1843 SNOMEDCT_US:399020009 SNOMEDCT_US:195021004 UMLS:C0007193
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|
| definition |
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.
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| has_alternative_id |
HP:0200130 HP:0005159 HP:0001725
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| has_exact_synonym |
Stretched and thinned heart muscle Cardiomyopathy, dilated DCM Congestive cardiomyopathy
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| has_obo_namespace |
human_phenotype
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|
| id |
HP:0001644
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|
| label |
Dilated cardiomyopathy
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|
| notation |
HP:0001644
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|
| prefLabel |
Dilated cardiomyopathy
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| treeView | ||
| subClassOf |
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