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 91 - 100 of 137 in total
Gene ID Gene Symbol Description Source
6390 SDHB succinate dehydrogenase complex iron sulfur subunit B
6392 SDHD succinate dehydrogenase complex subunit D
6514 SLC2A2 solute carrier family 2 member 2
6515 SLC2A3 solute carrier family 2 member 3
6517 SLC2A4 solute carrier family 2 member 4
6888 TALDO1 transaldolase 1
7355 SLC35A2 solute carrier family 35 member A2
7358 UGDH UDP-glucose 6-dehydrogenase
7378 UPP1 uridine phosphorylase 1
7412 VCAM1 vascular cell adhesion molecule 1
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
Related Glycoprotein

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: August 19, 2024