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 11 - 20 of 21 in total
Gene ID Gene Symbol Description Source
27306 HPGDS hematopoietic prostaglandin D synthase
54575 UGT1A10 UDP glucuronosyltransferase family 1 member A10
54576 UGT1A8 UDP glucuronosyltransferase family 1 member A8
54577 UGT1A7 UDP glucuronosyltransferase family 1 member A7
54578 UGT1A6 UDP glucuronosyltransferase family 1 member A6
54579 UGT1A5 UDP glucuronosyltransferase family 1 member A5
54600 UGT1A9 UDP glucuronosyltransferase family 1 member A9
54657 UGT1A4 UDP glucuronosyltransferase family 1 member A4
54658 UGT1A1 UDP glucuronosyltransferase family 1 member A1
54659 UGT1A3 UDP glucuronosyltransferase family 1 member A3
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