Disease #00013 (CPT2D (carnitine palmotoyltransferase 2 dificiency), OMIM:600650)

Zhejiang University Center for Genetic and Genomic Medicine (ZJU-CGGM)

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Official abbreviation	CPT2D
Name	carnitine palmotoyltransferase 2 dificiency
OMIM ID	600650
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 0 genes	-
Associated tissues	-
Disease features	-
Remarks	-