systemic primary carnitine deficiency disease

Summary
Synonym
  • carnitine transporter deficiency
  • carnitine uptake defect
  • deficiency of plasma-membrane carnitine transporter
  • primary carnitine deficiency
  • renal carnitine transport defect
Definition
An amino acid metabolic disorder that involves defective proteins called carnitine transporters, which bring carnitine into cells and prevent its escape from the body preventing the body cannot utilize fats for energy.
Super Class
amino acid metabolic disorder
External Links
Disease Ontology
DOID:14365
Mondo Disease Ontology
MeSH
UMLS
NCI Thesaurus
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 13 of 13 in total
Gene ID Gene Symbol Description Source
56994 CHPT1 choline phosphotransferase 1
57104 PNPLA2 patatin like phospholipase domain containing 2
79966 SCD5 stearoyl-CoA desaturase 5

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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