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 entries 1 - 10 of 21 in total
Gene ID Gene Symbol Description Source
28 ABO ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase
847 CAT catalase
2203 FBP1 fructose-bisphosphatase 1
2539 G6PD glucose-6-phosphate dehydrogenase
2592 GALT galactose-1-phosphate uridylyltransferase
2678 GGT1 gamma-glutamyltransferase 1
2821 GPI glucose-6-phosphate isomerase
2876 GPX1 glutathione peroxidase 1
3098 HK1 hexokinase 1
7355 SLC35A2 solute carrier family 35 member A2
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

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Last updated: August 19, 2024