Human Gene Set: HP_NEONATAL_OMPHALITIS


Standard name HP_NEONATAL_OMPHALITIS
Systematic name M46321
Brief description Neonatal omphalitis
Full description or abstract An infection of the umbilicus and/or surrounding tissues occurring in the neonatal period. [PMID:30020710]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0032435
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0032435
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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 2024.1.Hs: Updated to HPO Release 2024-04-26.

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