Disease #00502

Official abbreviation 616045
Name ?Combined oxidative phosphorylation deficiency 22, 616045 (3)
OMIM ID 616045
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 2 genes ATP5A1, ATP5F1A
Associated tissues -
Disease features -
Remarks -

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