Human Gene Set: HP_DILATED_CARDIOMYOPATHY


Standard name HP_DILATED_CARDIOMYOPATHY
Systematic name M35372
Brief description Dilated cardiomyopathy
Full description or abstract 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. [PMID:17916581]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0001644
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0001644
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Source species Homo sapiens
Contributed by Human Phenotype Ontology Group (The Jackson Laboratory (JAX))
Source platform or
identifier namespace		 Human_NCBI_Gene_ID
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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