All allelic disease phenotypes - locus/disease symbols
CPT2
carnitine palmitoyltransferase II
1p32
* Myopathy due to CPT II deficiency - CPT2 (9.15) * CPT deficiency, hepatic, type II - CPT2 (9.15) * Hypoglycemia hypoketonic, with deficiency of carnitine palmitoyltransferase II - CPTase (9.15)