Disease #00500

Official abbreviation	615595
Name	?Combined oxidative phosphorylation deficiency 19, 615595 (3)
OMIM ID	615595
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	LYRM4
Associated tissues	-
Disease features	-
Remarks	-