Human Gene Set: HP_ABNORMAL_PYRAMIDAL_TRACT_MORPHOLOGY


Standard name HP_ABNORMAL_PYRAMIDAL_TRACT_MORPHOLOGY
Systematic name M35614
Brief description Abnormal pyramidal tract morphology
Full description or abstract Any structural abnormality of the pyramidal tract, whose chief element, the corticospinal tract, is the only direct connection between the brain and the spinal cord. In addition to the corticospinal tract, the pyramidal system includes the corticobulbar, corticomesencephalic, and corticopontine tracts. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0002062
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0002062
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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: Renamed from HP_MORPHOLOGICAL_ABNORMALITY_OF_THE_PYRAMIDAL_TRACT. Updated to HPO Release 2024-04-26.

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