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 61 - 70 of 137 in total
Gene ID Gene Symbol Description Source
3948 LDHC lactate dehydrogenase C
3955 LFNG LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase
3957 LGALS2 galectin 2
3958 LGALS3 galectin 3
4023 LPL lipoprotein lipase
4099 MAG myelin associated glycoprotein
4153 MBL2 mannose binding lectin 2
4351 MPI mannose phosphate isomerase
4534 MTM1 myotubularin 1
4967 OGDH oxoglutarate dehydrogenase
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