SLC22A5 mutants

Stable Identifier
R-HSA-5625715
Type
Set [DefinedSet]
Species
Homo sapiens
Compartment
Locations in the PathwayBrowser
Participants
Disease
Name Identifier Synonyms
systemic primary carnitine deficiency disease 14365 carnitine uptake defect, carnitine transporter deficiency, primary carnitine deficiency, deficiency of plasma-membrane carnitine transporter, renal carnitine transport defect (disorder)