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Summary Literature (0)
MIM:616501 - MITOCHONDRIAL COMPLEX IV DEFICIENCY, NUCLEAR TYPE 13; MC4DN13

Xenbase Genes: coa6

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014668 - distal interphalangeal joint of manual digit 2
MONDO:0015487 - fatal infantile encephalocardiomyopathy

Disease Ontology (DO):
DOID:0080360 - mitochondrial complex IV deficiency nuclear type 13