Disease #03923

Official abbreviation COXPD-16
Name combined oxidative phosphorylation deficiency, type 16 (COXPD-16)
OMIM ID 615395
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MRPL44
Associated tissues -
Disease features -
Remarks -