Human Gene Set: HP_IMPAIRED_MASTICATION


Standard name HP_IMPAIRED_MASTICATION
Systematic name M36664
Brief description Impaired mastication
Full description or abstract An abnormal reduction in the ability to masticate (chew), i.e., in the ability to crush and ground food in preparation for swallowing. [PMID:23713640]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0005216
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0005216
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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 52 genes
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Show members (show 52 source identifiers mapped to 52 genes)
Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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