Disease #00528

Official abbreviation	615838
Name	Mitochondrial complex III deficiency, nuclear type 8, 615838 (3)
OMIM ID	615838
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	LYRM7
Associated tissues	-
Disease features	-
Remarks	-