RS1374482155 CPT2
Upload your DNA to see your genotype for this variant.
Associated Conditions
Carnitine palmitoyltransferase II deficiency
Carnitine palmitoyl transferase II deficiency
severe infantile form
Encephalopathy
acute
infection-induced
susceptibility to
4
neonatal form
myopathic form
Carnitine palmitoyltransferase II deficiency
Carnitine palmitoyl transferase II deficiency
severe infantile form
Encephalopathy
acute
Other Variants in CPT2