Human Gene Set: HP_BASAL_ENCEPHALOCELE


Standard name HP_BASAL_ENCEPHALOCELE
Systematic name M41421
Brief description Basal encephalocele
Full description or abstract Basal encephalocele is an encephalocele that occurs along the cribriform plate or through the sphenoid bone. The mass may appear in the nasal cavity, nasopharynx, epipharynx, sphenoid sinus, posterior orbit, or pterygopalatine fossa. The important distinction from other types is that no external tumor is visible except in those rare instances of herniations so large that they protrude through the mouth or nares. [https://orcid.org/0000-0002-0736-9199, PMID:4966739]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0011817
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0011817
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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 2023.1.Hs: Updated to HPO Release 2023-01-27.

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