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Summary Literature (0)
MIM:608836 - CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL

Xenbase Genes: cpt2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012136 - carnitine palmitoyl transferase II deficiency, neonatal form
MONDO:0015515 - carnitine palmitoyltransferase II deficiency

Disease Ontology (DO):
DOID:0060235 - carnitine palmitoyltransferase II deficiency