Disease #00014 (CACTD (carnitine-acylcarnitine translocase deficiency), OMIM:613698)

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

LOVD v.3.0 Build 29 [ Current LOVD status ]
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Official abbreviation	CACTD
Name	carnitine-acylcarnitine translocase deficiency
OMIM ID	613698
Human Phenotype Ontology Project (HPO)	HPO
Inheritance	-
Individuals reported having this disease	-
Phenotype entries for this disease	-
Associated with 1 gene	SLC25A20
Associated tissues	-
Disease features	-
Remarks	-