Disease #00563

Official abbreviation	617872
Name	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 34
OMIM ID	617872
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	MRPS7
Associated tissues	-
Disease features	-
Remarks	-