Human Gene Set: HP_MOTOR_AXONAL_NEUROPATHY


Standard name HP_MOTOR_AXONAL_NEUROPATHY
Systematic name M36970
Brief description Motor axonal neuropathy
Full description or abstract Progressive impairment of function of motor axons with muscle weakness, atrophy, and cramps. The deficits are length-dependent, meaning that muscles innervated by the longest nerves are affected first, so that for instance the arms are affected at a later age than the onset of deficits involving the lower leg. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0007002
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0007002
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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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