Human Gene Set: HP_HEMOLYTIC_UREMIC_SYNDROME


Standard name HP_HEMOLYTIC_UREMIC_SYNDROME
Systematic name M36738
Brief description Hemolytic-uremic syndrome
Full description or abstract A thrombotic microangiopathy with presence of non-immune, intravascular hemolytic anemia, thrombocytopenia and acute kidney injury. A vicious cycle of complement activation, endothelial cell damage, platelet activation, and thrombosis is the hallmark of the disease. [PMID:19846853, PMID:28416508]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0005575
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0005575
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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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GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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