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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
placental insufficiency
Summary
- Definition
- A placenta disease that is characterized by insufficient blood flow to the placenta during pregnancy.
- Super Class
- placenta disease
External Links
- Disease Ontology
- DOID:3891
- Mondo Disease Ontology
- MeSH
- UMLS
- MGI genotype (from TogoID)
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 1727 | CYB5R3 | cytochrome b5 reductase 3 | |
| 1737 | DLAT | dihydrolipoamide S-acetyltransferase | |
| 1836 | SLC26A2 | solute carrier family 26 member 2 | |
| 2182 | ACSL4 | acyl-CoA synthetase long chain family member 4 | |
| 2218 | FKTN | fukutin | |
| 2220 | FCN2 | ficolin 2 | |
| 2530 | FUT8 | fucosyltransferase 8 | |
| 2538 | G6PC1 | glucose-6-phosphatase catalytic subunit 1 | |
| 2581 | GALC | galactosylceramidase | |
| 2584 | GALK1 | galactokinase 1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q9Y487 | V-type proton ATPase 116 kDa subunit a 2 | |
| Q9Y5X9 | Endothelial lipase | |
| Q9Y6A1 | Protein O-mannosyl-transferase 1 |
