Human Gene Set: HP_GAIT_DISTURBANCE


Standard name HP_GAIT_DISTURBANCE
Systematic name M35215
Brief description Gait disturbance
Full description or abstract The term gait disturbance can refer to any disruption of the ability to walk. In general, this can refer to neurological diseases but also fractures or other sources of pain that is triggered upon walking. However, in the current context gait disturbance refers to difficulty walking on the basis of a neurological or muscular disease. [https://orcid.org/0000-0002-0736-9199, PMID:27770207]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0001288
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0001288
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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
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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