Human Gene Set: HP_ABNORMAL_CORTICOSPINAL_TRACT_MORPHOLOGY


Standard name HP_ABNORMAL_CORTICOSPINAL_TRACT_MORPHOLOGY
Systematic name M35858
Brief description Abnormal corticospinal tract morphology
Full description or abstract Abnormality of the corticospinal tract, which is the chief element of the pyramidal system (the principle motor tract) and is the only direct connection between the cerebrum and the spinal cord. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0002492
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External links https://hpo.jax.org/app/browse/term/HP:0002492
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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_CORTICOSPINAL_TRACT. Updated to HPO Release 2024-04-26.

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