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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 |
|---|---|---|---|
| 8050 | PDHX | pyruvate dehydrogenase complex component X | |
| 8547 | FCN3 | ficolin 3 | |
| 8985 | PLOD3 | procollagen-lysine,2-oxoglutarate 5-dioxygenase 3 | |
| 9126 | SMC3 | structural maintenance of chromosomes 3 | |
| 9197 | SLC33A1 | solute carrier family 33 member 1 | |
| 9365 | KL | klotho | |
| 9382 | COG1 | component of oligomeric golgi complex 1 | |
| 9388 | LIPG | lipase G, endothelial type | |
| 9563 | H6PD | hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase | |
| 9791 | PTDSS1 | phosphatidylserine synthase 1 |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q12860 | Contactin-1 | |
| Q12918 | Killer cell lectin-like receptor subfamily B member 1 | |
| Q13085 | Acetyl-CoA carboxylase 1 | |
| Q13563 | Polycystin-2 | |
| Q15392 | Delta(24)-sterol reductase | |
| Q15485 | Ficolin-2 | |
| Q16831 | Uridine phosphorylase 1 | |
| Q16836 | Hydroxyacyl-coenzyme A dehydrogenase, mitochondrial | |
| Q5H8A4 | GPI ethanolamine phosphate transferase 2 | |
| Q6NSJ0 | Myogenesis-regulating glycosidase |
