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
Displaying entries 1 - 10 of 137 in total
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
Displaying all 2 entries
Gene ID Gene Symbol Description Source
18609 Pdx1 pancreatic and duodenal homeobox 1
19017 Ppargc1a peroxisome proliferative activated receptor, gamma, coactivator 1 alpha
Displaying all 2 entries
Gene ID Gene Symbol Description Source
29535 Pdx1 pancreatic and duodenal homeobox 1
83516 Ppargc1a PPARG coactivator 1 alpha

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024