Disease #00076

Official abbreviation COXPD8
Name COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 8; COXPD8
OMIM ID 614096
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene AARS2
Associated tissues -
Disease features -
Remarks -