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
00037 MC3DN-1 mitochondrial complex III deficiency, nuclear, type 1 (MC3DN-1)] 124000 - - - BCS1L, UQCRC2 - -
03845 MC3DN-5 mitochondrial complex III deficiency, nuclear type 5 (MC3DN-5) 615160 - - - UQCRC2 - -
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