Disease #00565

Official abbreviation	617950
Name	COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 36
OMIM ID	617950
Human Phenotype Ontology Project (HPO)	HPO
Individuals reported having this disease	0
Phenotype entries for this disease	0
Associated with 1 gene	MRPS2
Associated tissues	-
Disease features	-
Remarks	-