RS373638740 CPT2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Carnitine palmitoyl transferase II deficiency
severe infantile form
Carnitine palmitoyltransferase II deficiency
Encephalopathy
acute
infection-induced
susceptibility to
4
CPT2-related disorder
neonatal form
myopathic form
Inborn genetic diseases
Carnitine palmitoyl transferase II deficiency
severe infantile form
Carnitine palmitoyltransferase II deficiency
Other Variants in CPT2