Human Gene Set: HP_SIMPLIFIED_GYRAL_PATTERN


Standard name HP_SIMPLIFIED_GYRAL_PATTERN
Systematic name M37449
Brief description Simplified gyral pattern
Full description or abstract An abnormality of the cerebral cortex with fewer gyri but with normal cortical thickness. This pattern is usually often associated with congenital microcephaly. [http://www.wikidata.org/entity/Q90573458, https://orcid.org/0000-0002-0736-9199, PMID:22427329]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0009879
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0009879
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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
Dataset references  
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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