Human Gene Set: HP_SINGLE_LINEAGE_MYELODYSPLASIA


Standard name HP_SINGLE_LINEAGE_MYELODYSPLASIA
Systematic name M45451
Brief description Single lineage myelodysplasia
Full description or abstract Abnormality/dysplasia of a single myeloid cell (erythroid, granulocytic, or megakaryocytic). [https://orcid.org/0000-0003-2945-4463]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0012150
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0012150
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
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Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)

Legacy heatmaps (PNG)
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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