RS1009503062 CPT2

Health Risk Chr 1:53213510

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Associated Conditions

Carnitine palmitoyl transferase II deficiency

severe infantile form

myopathic form

neonatal form

Encephalopathy

acute

infection-induced

susceptibility to

4

Carnitine palmitoyltransferase II deficiency

Inborn genetic diseases

Carnitine palmitoyl transferase II deficiency

severe infantile form

myopathic form

neonatal form

Other Variants in CPT2

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