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
04131 COXPD21 combined oxidative phosphorylation deficiency, type 21 (COXPD-21) 615918 AR - - TARS2 - -
06682 TTD7 Trichothiodystrophy 7, nonphotosensitive 618546 AR - - TARS - -
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