Human Gene Set: HP_PROLONGED_NEONATAL_JAUNDICE


Standard name HP_PROLONGED_NEONATAL_JAUNDICE
Systematic name M36885
Brief description Prolonged neonatal jaundice
Full description or abstract Neonatal jaundice refers to a yellowing of the skin and other tissues of a newborn infant as a result of increased concentrations of bilirubin in the blood. Neonatal jaundice affects over half of all newborns to some extent in the first week of life. Prolonged neonatal jaundice is said to be present if the jaundice persists for longer than 14 days in term infants and 21 days in preterm infants. [https://orcid.org/0000-0002-0736-9199]
Collection C5: Ontology
      HPO: Human Phenotype Ontology
Source publication  
Exact source HP:0006579
Related gene sets  
External links https://hpo.jax.org/app/browse/term/HP:0006579
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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 2026.1.Hs: Updated to HPO Release 2026-01-08.


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