Human Gene Set: HP_ABNORMALITY_OF_THE_PHARYNX


Standard name HP_ABNORMALITY_OF_THE_PHARYNX
Systematic name M34827
Brief description Abnormality of the pharynx
Full description or abstract An anomaly of the pharynx, i.e., of the tubular structure extending from the base of the skull superiorly to the esophageal inlet inferiorly. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0000600
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0000600
Filtered by similarity ? (show 1 similar ontology term(s) from the external resource)
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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NCI-60 cell lines (National Cancer Institute)
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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