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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:Histiocytoid cardiomyopathy
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Accession:HP:0005152 term browser browse the term
Definition:A type of cardiomyopathy characterized pathologically by hamartomatous lesions of cardiac Purkinje cells.
Comment:This HPO term intends to refer to the histological changes that characterize histiocytoid cardiomyopthy. The disease entity Histiocytoid cardiomyopathy is a rare arrhythmogenic disorder characterized by incessant ventricular tachycardia, cardiomegaly, and often sudden death by age 2 years.
Synonyms:exact_synonym: Arachnocytosis of the myocardium;   Foamy myocardial transformation;   Focal lipid cardiomyopathy;   Infantile cardiomyopathy with histiocytoid changes;   Infantile xanthomatous cardiomyopathy;   Isolated cardiac lipidosis;   Myocardial or conduction system hamartoma;   Oncocytic cardiomyopathy
 xref: UMLS:C1708371


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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
                Histiocytoid cardiomyopathy 0
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