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
04506 MMDS3 mitochondrial dysfunctions, multiple, syndrome, type 3 615330 AR - - IBA57 - -
04507 SPG74 paraplegia, spastic?, autosomal recessive, type 74 (SPG-74) 616451 AR - - IBA57 - -
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