All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00321 MC5DN2 mitochondrial complex V (ATP synthase) deficiency, nuclear, type 2 (MC5DN-2) 614052 AR 1 1 TMEM70 - -
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