Disease #00437

Official abbreviation	CACTD
Name	CARNITINE-ACYLCARNITINE TRANSLOCASE DEFICIENCY;CACTD
OMIM ID	212138
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	SLC25A20
Associated tissues	-
Disease features	-
Remarks	-