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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:Cardiomyopathy
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Accession:HP:0001638 term browser browse the term
Definition: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.
Synonyms:exact_synonym: Disease of the heart muscle
 xref: Fyler:1840;   MESH:D009202;   SNOMEDCT_US:57809008;   SNOMEDCT_US:85898001;   UMLS:C0878544


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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
                Atrial cardiomyopathy 0
                Dilated cardiomyopathy 0
                Histiocytoid cardiomyopathy 0
                Hypertrophic cardiomyopathy + 0
                Noncompaction cardiomyopathy + 0
                Restrictive cardiomyopathy 0
                Right ventricular cardiomyopathy 0
                Takotsubo cardiomyopathy 0
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