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
03378 C1QD C1q deficiency 613652 AR - - C1QA, C1QB, C1QC - -
06347 COXPD33 Combined oxidative phosphorylation deficiency 33 617713 AR - - C1QBP - -
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