RS74315295 CPT2
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What This Variant Does
"[OMIM:?]
Associated Conditions
Carnitine palmitoyl transferase II deficiency
myopathic form
severe infantile form
Carnitine palmitoyltransferase II deficiency
neonatal form
Encephalopathy
acute
infection-induced
susceptibility to
4
Seizure
Abnormality of the nervous system
Carnitine palmitoyl transferase II deficiency
myopathic form
severe infantile form
Other Variants in CPT2