Human Gene Set: HP_ABNORMALITY_OF_NEURONAL_MIGRATION


Standard name HP_ABNORMALITY_OF_NEURONAL_MIGRATION
Systematic name M35745
Brief description Abnormality of neuronal migration
Full description or abstract An abnormality resulting from an anomaly of neuronal migration, i.e., of the process by which neurons travel from their origin to their final position in the brain. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0002269
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0002269
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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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