Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (0)
MIM:614052 - MITOCHONDRIAL COMPLEX V (ATP SYNTHASE) DEFICIENCY, NUCLEAR TYPE 2; MC5DN2

Xenbase Genes: tmem70

Human Disease Resource: OMIM

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