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congenital heart disease
Summary
- Synonym
-
- Congenital Heart Defects
- Congenital anomaly of heart
- Heart Malformation
- congenital heart defect
- heart defect
- Definition
- A heart disease that is characterized by problems with the heart's structure that are present at birth.
- Super Class
- heart disease physical disorder
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 7044 | LEFTY2 | left-right determination factor 2 | |
| 7092 | TLL1 | tolloid like 1 | |
| 7422 | VEGFA | vascular endothelial growth factor A | |
| 23118 | TAB2 | TGF-beta activated kinase 1 (MAP3K7) binding protein 2 | |
| 23543 | RBFOX2 | RNA binding fox-1 homolog 2 | |
| 27086 | FOXP1 | forkhead box P1 | |
| 171019 | ADAMTS19 | ADAM metallopeptidase with thrombospondin type 1 motif 19 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| P28700 | Retinoic acid receptor RXR-alpha | |
| Q8BIH0 | Histone deacetylase complex subunit SAP130 |
| UniProt ID | Protein Name | Source |
|---|---|---|
| B7Z002 | Kismet, isoform C | |
| P20659 | Histone-lysine N-methyltransferase trithorax | |
| Q9V496 | Apolipophorins | |
| Q9V4C8 | Host cell factor |
| UniProt ID | Protein Name | Source |
|---|---|---|
| A0A8M9QJ57 | Voltage-dependent L-type calcium channel subunit alpha | |
| Q5RGJ8 | N-acetylglucosamine-1-phosphotransferase subunits alpha/beta |
