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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 |
|---|---|---|---|
| 28 | ABO | ABO, alpha 1-3-N-acetylgalactosaminyltransferase and alpha 1-3-galactosyltransferase | |
| 31 | ACACA | acetyl-CoA carboxylase alpha | |
| 37 | ACADVL | acyl-CoA dehydrogenase very long chain | |
| 125 | ADH1B | alcohol dehydrogenase 1B (class I), beta polypeptide | |
| 175 | AGA | aspartylglucosaminidase | |
| 217 | ALDH2 | aldehyde dehydrogenase 2 family member | |
| 218 | ALDH3A1 | aldehyde dehydrogenase 3 family member A1 | |
| 231 | AKR1B1 | aldo-keto reductase family 1 member B | |
| 308 | ANXA5 | annexin A5 | |
| 523 | ATP6V1A | ATPase H+ transporting V1 subunit A |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| O75636 | Ficolin-3 | |
| O95479 | GDH/6PGL endoplasmic bifunctional protein | |
| P00325 | All-trans-retinol dehydrogenase [NAD(+)] ADH1B | |
| P00387 | NADH-cytochrome b5 reductase 3 | |
| P04040 | Catalase | |
| P04062 | Lysosomal acid glucosylceramidase | |
| P04156 | Major prion protein | |
| P04233 | HLA class II histocompatibility antigen gamma chain | |
| P04406 | Glyceraldehyde-3-phosphate dehydrogenase | |
| P04798 | Cytochrome P450 1A1 |
