carnitine deficiency, systemic primary Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/212140
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Genes

1 genes associated with the carnitine deficiency, systemic primary phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
SLC22A5 solute carrier family 22 (organic cation/carnitine transporter), member 5