Disease #00405

Official abbreviation	238710
Name	HYPERLYSINEMIA DUE TO DEFECT IN LYSINE TRANSPORT INTO MITOCHONDRIA
OMIM ID	238710
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 0 genes	-
Associated tissues	-
Disease features	-
Remarks	-