Disease #00423

Official abbreviation	COXPD11
Name	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 11; COXPD11
OMIM ID	614922
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	RMND1
Associated tissues	-
Disease features	-
Remarks	-