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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 |
|---|---|---|---|
| 3030 | HADHA | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit alpha | |
| 3032 | HADHB | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | |
| 3033 | HADH | hydroxyacyl-CoA dehydrogenase | |
| 3037 | HAS2 | hyaluronan synthase 2 | |
| 3098 | HK1 | hexokinase 1 | |
| 3291 | HSD11B2 | hydroxysteroid 11-beta dehydrogenase 2 | |
| 3292 | HSD17B1 | hydroxysteroid 17-beta dehydrogenase 1 | |
| 3482 | IGF2R | insulin like growth factor 2 receptor | |
| 3651 | PDX1 | pancreatic and duodenal homeobox 1 | |
| 3820 | KLRB1 | killer cell lectin like receptor B1 |
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 |
