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MIM:608836 - CARNITINE PALMITOYLTRANSFERASE II DEFICIENCY, LETHAL NEONATAL
Echinobase Genes: cpt2
Human Disease Resource: OMIM
DOID:0060235 - carnitine palmitoyltransferase II deficiency |
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DOID:0060235 - carnitine palmitoyltransferase II deficiency |