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Summary Literature (0)
MIM:617228 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 31; COXPD31

Xenbase Genes: mipep

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014976 - lethal left ventricular non-compaction-seizures-hypotonia-cataract-developmental delay syndrome

Disease Ontology (DO):
DOID:0111488 - combined oxidative phosphorylation deficiency 31