All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00168 PHARC polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract (PHARC) 612674 - 32 26 ABHD12 - -
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