RS144760921 CPT2
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Associated Conditions
Carnitine palmitoyltransferase II deficiency
Carnitine palmitoyl transferase II deficiency
neonatal form
Encephalopathy
acute
infection-induced
susceptibility to
4
severe infantile form
myopathic form
Inborn genetic diseases
CPT2-related disorder
Carnitine palmitoyltransferase II deficiency
Carnitine palmitoyl transferase II deficiency
neonatal form
Other Variants in CPT2