Disease #00411

Official abbreviation COXPD6
Name COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6
OMIM ID 300816
Human Phenotype Ontology Project (HPO) HPO
Individuals reported having this disease 0
Phenotype entries for this disease 0
Associated with 1 gene AIFM1
Associated tissues -
Disease features -
Remarks -

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