Disease #00493

Official abbreviation COXPD7
Name COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 7; COXPD7
OMIM ID 613559
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene C12orf65
Associated tissues -
Disease features -
Remarks -

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