Human Gene Set: HP_HYPERTROPHIC_CARDIOMYOPATHY


Standard name HP_HYPERTROPHIC_CARDIOMYOPATHY
Systematic name M35367
Brief description Hypertrophic cardiomyopathy
Full description or abstract Hypertrophic cardiomyopathy (HCM) is defined by the presence of increased ventricular wall thickness or mass in the absence of loading conditions (hypertension, valve disease) sufficient to cause the observed abnormality. [PMID:17916581]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0001639
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0001639
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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
Dataset references  
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Version history 2026.1.Hs: Updated to HPO Release 2026-01-08.


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