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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 |
|---|---|---|---|
| 3948 | LDHC | lactate dehydrogenase C | |
| 3955 | LFNG | LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase | |
| 3957 | LGALS2 | galectin 2 | |
| 3958 | LGALS3 | galectin 3 | |
| 4023 | LPL | lipoprotein lipase | |
| 4099 | MAG | myelin associated glycoprotein | |
| 4153 | MBL2 | mannose binding lectin 2 | |
| 4351 | MPI | mannose phosphate isomerase | |
| 4534 | MTM1 | myotubularin 1 | |
| 4967 | OGDH | oxoglutarate dehydrogenase |
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 |
