- OMIM ID
-
608836
- OMIM term:
- CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL
- Alternative terms:
-
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, NEONATAL
CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, ANTENATAL
CPT II DEFICIENCY, LETHAL NEONATAL
CPT2 DEFICIENCY, LETHAL NEONATAL
- (∗) Location:
- 1p32.3
- (†) Associated OMIM genes:
- CPT2
- (‡) Associated MGI genes:
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