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
03967 NDGOA neurodegeneration, with optic atrophy, childhood-onset (NDGOA) 615491 AR - - UCHL1 - -
03375 PARK5 Parkinson disease, type 5 (PARK-5) 613643 AD - - UCHL1 - -
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