Disease #00098

Official abbreviation	COXPD4
Name	Combined oxidative phosphorylation deficiency 4, 610678 (3)
OMIM ID	610678
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	TUFM
Associated tissues	-
Disease features	-
Remarks	-