Disease #00157

Official abbreviation	500003
Name	STRIATONIGRAL DEGENERATION, INFANTILE, MITOCHONDRIAL
OMIM ID	500003
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	MT-ATP6
Associated tissues	-
Disease features	-
Remarks	-