Disease #00473

Official abbreviation	CDSP
Name	CARNITINE DEFICIENCY, SYSTEMIC PRIMARY; CDSP
OMIM ID	212140
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	SLC22A5
Associated tissues	-
Disease features	-
Remarks	-