- OMIM ID
-
600649
- OMIM term:
- CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE
- Alternative terms:
-
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY WITH HYPOKETOTIC HYPOGLYCEMIA
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, HEPATOCARDIOMUSCULAR
CPT II DEFICIENCY, HEPATIC
CPT2 DEFICIENCY, INFANTILE
- (∗) Location:
- 1p32.3
- (†) Associated OMIM genes:
- CPT2
- (‡) Associated MGI genes:
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