RS754363068 CPT2

Health Risk Chr 1:53197050

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Associated Conditions

Carnitine palmitoyl transferase II deficiency

myopathic form

severe infantile form

neonatal form

Carnitine palmitoyltransferase II deficiency

Encephalopathy

acute

infection-induced

susceptibility to

4

Inborn genetic diseases

Carnitine palmitoyl transferase II deficiency

myopathic form

severe infantile form

neonatal form

Other Variants in CPT2

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