Disease #02951 (COXPD-2 (combined oxidative phosphorylation deficiency, type 2 (COXPD-2)), OMIM:610498)

Official abbreviation COXPD-2
Name combined oxidative phosphorylation deficiency, type 2 (COXPD-2)
OMIM ID 610498
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MRPS16
Associated tissues -
Disease features -
Remarks -