Human Gene Set: HP_ABNORMAL_ERYTHROID_LINEAGE_CELL_MORPHOLOGY


Standard name HP_ABNORMAL_ERYTHROID_LINEAGE_CELL_MORPHOLOGY
Systematic name M48819
Brief description Abnormal erythroid lineage cell morphology
Full description or abstract An anomaly of erythroid lineage cells, that is, of the erythropoietic cells in the lineage leading to and including erythrocytes. [https://orcid.org/0000-0003-2945-4463]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0012130
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0012130
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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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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