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
01133 COXPD13 combined oxidative phosphorylation deficiency, type 13 (COXPD-13) 614932 AR - - PNPT1 - -
01134 DFNB70 deafness, autosomal recessive, type 70 (DFNB-70) 614934 AR - - PNPT1 - -
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