Human Gene Set: HP_ARRHINENCEPHALY


Standard name HP_ARRHINENCEPHALY
Systematic name M35664
Brief description Arrhinencephaly
Full description or abstract A defect of development of the brain characterized by congenital absence of the part of the brain that includes the olfactory bulbs, tracts, and other structures associated with the sense of smell. []
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0002139
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0002139
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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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GTEx compendium
Human tissue compendium (Novartis)
Global Cancer Map (Broad Institute)
NCI-60 cell lines (National Cancer Institute)
Advanced query Further investigate these 34 genes
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Show members (show 34 source identifiers mapped to 34 genes)
Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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