Disease #04014

Official abbreviation COXPD-18
Name combined oxidative phosphorylation deficiency, type 18 (COXPD-18)
OMIM ID 615578
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene SFXN4
Associated tissues -
Disease features -
Remarks -