Disease #00512

Official abbreviation	614932
Name	Combined oxidative phosphorylation deficiency 13, 614932 (3)
OMIM ID	614932
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	PNPT1
Associated tissues	-
Disease features	-
Remarks	-