Disease #00025

Official abbreviation 614053
Name Mitochondrial complex V (ATP synthase) deficiency, nuclear type 3, 614053 (3)
OMIM ID 614053
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 2 genes ATP5E, ATP5F1E
Associated tissues -
Disease features -
Remarks -

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