RS144658100 CPT2
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Associated Conditions
Carnitine palmitoyl transferase II deficiency
severe infantile form
Encephalopathy
acute
infection-induced
susceptibility to
4
myopathic form
neonatal form
Carnitine palmitoyltransferase II deficiency
CPT2-related disorder
Inborn genetic diseases
Carnitine palmitoyl transferase II deficiency
severe infantile form
Encephalopathy
Other Variants in CPT2