Disease #00466

Official abbreviation	CPT II
Name	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, INFANTILE;CPT2
OMIM ID	600649
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 2 genes	, CPT2
Associated tissues	-
Disease features	-
Remarks	-