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GTR Home > Conditions/Phenotypes > Combined oxidative phosphorylation deficiency 22

Combined oxidative phosphorylation deficiency 22

Available tests

14 tests are in the database for this condition.

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Clinical tests (14 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: ATP5A, ATP5A1, ATP5AL2, ATPM, COXPD22, HEL-S-123m, MC5DN4, MC5DN4A, MC5DN4B, MOM2, OMR, ORM, hATP1, ATP5F1A
    Summary: ATP synthase F1 subunit alpha

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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