Human Gene Set: HP_ACUTE_CORONARY_SYNDROME


Standard name HP_ACUTE_CORONARY_SYNDROME
Systematic name M48891
Brief description Acute coronary syndrome
Full description or abstract The term acute coronary syndrome (ACS) refers to any group of clinical symptoms compatible with acute myocardial ischemia and includes unstable angina (UA), non-ST-segment elevation myocardial infarction (NSTEMI), and ST-segment elevation myocardial infarction (STEMI). [PMID:19797781]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0033678
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0033678
Filtered by similarity ? (show 1 similar ontology term(s) from the external resource)
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 2024.1.Hs: Updated to HPO Release 2024-04-26.

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