Disease #00095

Official abbreviation COXPD15
Name Combined oxidative phosphorylation deficiency 15, 614947 (3)
OMIM ID 614947
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene MTFMT
Associated tissues -
Disease features -
Remarks -

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