Disease #00487

Official abbreviation	608836
Name	CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL
OMIM ID	608836
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	CPT2
Associated tissues	-
Disease features	-
Remarks	-