All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
07144 OPA12 optic atrophy, type 12 618977 AD - - AFG3L2 - -
02920 SCA28 ataxia, spinocerebellar, type 28 (SCA-28) 610246 AD 6 5 AFG3L2 - -
03663 SPAX5 ataxia, spastic, type 5, autosomal recessive (SPAX-5) 614487 AR - - AFG3L2 - -
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