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
03362 COXPD7 combined oxidative phosphorylation deficiency, type 7 (COXPD-7) 613559 AR 1 1 C12orf65 - -
04388 SPG55 paraplegia, spastic, autosomal recessive, type 55 (SPG-55) 615035 AR - - C12orf65 - -
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