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GTR Home > Conditions/Phenotypes > Combined oxidative phosphorylation deficiency 19

Combined oxidative phosphorylation deficiency 19

Summary

Any combined oxidative phosphorylation deficiency in which the cause of the disease is a mutation in the LYRM4 gene. [from MONDO]

Available tests

9 tests are in the database for this condition.

Check Related conditions for additional relevant tests.

Clinical tests (9 available)

Molecular Genetics Tests

Genes See tests for all associated and related genes

  • Also known as: C6orf149, CGI-203, COXPD19, ISD11, LYRM4
    Summary: LYR motif containing 4

Clinical features

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Imported from Human Phenotype Ontology (HPO)

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