All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04590 COXPD24 oxidative phosphorylation deficiency, combined, type 24 (COXPD-24) 616239 AR - - NARS2 - -
06142 DFNB94 ?Deafness, autosomal recessive 94 618434 AR - - NARS2 - -
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