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 101 - 110 of 137 in total
Gene ID Gene Symbol Description Source
8050 PDHX pyruvate dehydrogenase complex component X
8547 FCN3 ficolin 3
8985 PLOD3 procollagen-lysine,2-oxoglutarate 5-dioxygenase 3
9126 SMC3 structural maintenance of chromosomes 3
9197 SLC33A1 solute carrier family 33 member 1
9365 KL klotho
9382 COG1 component of oligomeric golgi complex 1
9388 LIPG lipase G, endothelial type
9563 H6PD hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase
9791 PTDSS1 phosphatidylserine synthase 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

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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