Human Gene Set: HP_ERYTHROID_HYPOPLASIA


Standard name HP_ERYTHROID_HYPOPLASIA
Systematic name M38023
Brief description Erythroid hypoplasia
Full description or abstract Decreased count of erythroid precursor cells, that is, erythroid lineage cells in the bone marrow. [https://orcid.org/0000-0003-2945-4463]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0012133
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0012133
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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)
Advanced query Further investigate these 31 genes
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Show members (show 31 source identifiers mapped to 31 genes)
Version history 2023.1.Hs: Updated to HPO Release 2023-01-27.

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