Human Gene Set: HP_ABNORMALITY_OF_THE_CHIN


Standard name HP_ABNORMALITY_OF_THE_CHIN
Systematic name M34657
Brief description Abnormality of the chin
Full description or abstract An abnormality of the chin, i.e., of the inferior portion of the face lying inferior to the lower lip and including the central prominence of the lower jaw. [https://orcid.org/0000-0002-0736-9199, PMID:19125436]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0000306
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0000306
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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
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Version history 2024.1.Hs: Updated to HPO Release 2024-04-26.

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