Human Gene Set: HP_HEMIPLEGIA


Standard name HP_HEMIPLEGIA
Systematic name M35758
Brief description Hemiplegia
Full description or abstract Paralysis (complete loss of muscle function) in the arm, leg, and in some cases the face on one side of the body. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0002301
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0002301
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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 39 genes
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Show members (show 39 source identifiers mapped to 39 genes)
Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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