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Standards Ontologies Notations
congenital heart disease

Summary
Synonym
  • Congenital Heart Defects
  • Congenital anomaly of heart
  • Heart Malformation
  • congenital heart defect
  • heart defect
Super Class
heart disease physical disorder
External Links
Disease Ontology
DOID:1682
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying entries 21 - 30 of 43 in total
Gene ID Gene Symbol Description Source
5743 PTGS2 prostaglandin-endoperoxide synthase 2
6309 SC5D sterol-C5-desaturase
6403 SELP selectin P
6470 SHMT1 serine hydroxymethyltransferase 1
6515 SLC2A3 solute carrier family 2 member 3
8692 HYAL2 hyaluronidase 2
8794 TNFRSF10C TNF receptor superfamily member 10c
9993 DGCR2 DiGeorge syndrome critical region gene 2
10682 EBP EBP cholestenol delta-isomerase
11091 WDR5 WD repeat domain 5
Displaying 1 entry
Gene ID Gene Symbol Description Source
140858 Wdr5 WD repeat domain 5
Displaying 1 entry
Gene ID Gene Symbol Description Source
362093 Wdr5 WD repeat domain 5
Displaying all 2 entries
Gene ID Gene Symbol Description Source
31293 N Notch
43565 Axn Axin
Related Glycoprotein
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International Collaboration

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