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Summary Literature (0)
MIM:614052 - MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2

Xenbase Genes: tmem70

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013546 - mitochondrial complex V (ATP synthase) deficiency, nuclear type 2

Disease Ontology (DO):
DOID:0060331 - mitochondrial complex V (ATP synthase) deficiency nuclear type 2