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
04447 ACPHD ataxia?, combined cerebellar and peripheral, with hearing loss and diabetes mellitus (ACPHD) 616192 AR - - DNAJC3 - -
02274 LHON Leber hereditary optic neuropathy 535000 AR;Mi 78 63 DNAJC30, MT-ND1 - -
06968 LHONAR Leber hereditary optic neuropathy, autosomal recessive autosomal recessive 619382 AR - - DNAJC30 - -
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