Disease #03950

Official abbreviation COXPD-17
Name combined oxidative phosphorylation deficiency, type 17 (COXPD-17)
OMIM ID 615440
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene ELAC2
Associated tissues -
Disease features -
Remarks -