Human Gene Set: HP_PARAPLEGIA


Standard name HP_PARAPLEGIA
Systematic name M37577
Brief description Paraplegia
Full description or abstract Severe or complete weakness of both lower extremities with sparing of the upper extremities. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0010550
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0010550
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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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NCI-60 cell lines (National Cancer Institute)
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Version history 2026.1.Hs: Updated to HPO Release 2026-01-08.


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