Disease #00100

Official abbreviation COXPD9
Name Combined oxidative phosphorylation deficiency 9, 614582 (3)
OMIM ID 614582
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MRPL3
Associated tissues -
Disease features -
Remarks -