All diseases

OMIM ID
255120
OMIM term:
CARNITINE PALMITOYLTRANSFERASE I DEFICIENCY
Alternative terms:
CARNITINE PALMITOYLTRANSFERASE IA DEFICIENCY
CPT I DEFICIENCY
CPT DEFICIENCY, HEPATIC, TYPE I
(∗) Location:
11q13.3  
(†) Associated OMIM genes:
CPT1A  
(‡) Associated MGI genes:
Cpt1a  

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