Disease #00523

Official abbreviation	617664
Name	Combined oxidative phosphorylation deficiency 32, 617664 (3)
OMIM ID	617664
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	MRPS34
Associated tissues	-
Disease features	-
Remarks	-