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
05363 ANOA;MMDS9A neuropathy, auditory, and optic atrophy 617717 AR 4 4 FDXR - autosomal recessive
07137 MMDS9B mitochondrial dysfunctions, multiple, syndrome, type 9B 620887 AR - - FDXR - -
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