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HUMAN PHENOTYPE - ANNOTATIONS

The Human Phenotype Ontology (HPO) is downloaded weekly from http://compbio.charite.de/hudson/job/hpo/lastStableBuild/artifact/ontology/release/hp.obo. The file downloaded is considered the "last stable build" available for the ontology. For more about the HPO, view their website at http://www.human-phenotype-ontology.org/.
Term:Dilated cardiomyopathy
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Accession:HP:0001644 term browser browse the term
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.
Synonyms:exact_synonym: Congestive cardiomyopathy;   DCM;   Stretched and thinned heart muscle
 narrow_synonym: idiopathic dilated cardiomyopathy
 alt_id: HP:0001725;   HP:0005159;   HP:0200130
 xref: EFO:0000407;   EFO:0009094;   Fyler:1843;   SNOMEDCT_US:195021004;   SNOMEDCT_US:399020009;   UMLS:C0007193


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  Human phenotype 0
    Phenotypic abnormality 0
      Abnormality of the cardiovascular system 0
        Abnormal cardiovascular system morphology 0
          Abnormal heart morphology 0
            Abnormal myocardium morphology 0
              Cardiomyopathy 0
                Dilated cardiomyopathy 0
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