Disease #00099

Official abbreviation COXPD5
Name Combined oxidative phosphorylation deficiency 5, 611719 (3)
OMIM ID 611719
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MRPS22
Associated tissues -
Disease features -
Remarks -

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