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Standards Ontologies Notations
neonatal jaundice

Summary
Synonym
  • neonatal hyperbilirubinemia
  • neonatal icterus
Definition
A pigmentation disease characterized by a high level of bilirubin in the blood, causing a yellowing of the skin and other tissues of a newborn infant.
Super Class
pigmentation disease
External Links
Disease Ontology
DOID:2383
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
MGI genotype (from TogoID)
Related Genes
Displaying entry 21 - 21 of 21 in total
Gene ID Gene Symbol Description Source
56886 UGGT1 UDP-glucose glycoprotein glucosyltransferase 1
Displaying all 2 entries
Gene ID Gene Symbol Description Source
14380 G6pd2 glucose-6-phosphate dehydrogenase 2
14381 G6pdx glucose-6-phosphate dehydrogenase X-linked
Displaying 1 entry
Gene ID Gene Symbol Description Source
24377 G6pd glucose-6-phosphate dehydrogenase
Displaying 1 entry
Gene ID Gene Symbol Description Source
32974 Zw Zwischenferment
Displaying 1 entry
Gene ID Gene Symbol Description Source
178046 gspd-1 Glucose-6-phosphate 1-dehydrogenase
Displaying 1 entry
Gene ID Gene Symbol Description Source
855480 ZWF1 glucose-6-phosphate dehydrogenase
Related Glycoprotein
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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01

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Last updated: August 19, 2024