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
01339 - fundus albipunctatus (retinitis punctata albescens (RPA)) 136880 AD;AR 110 110 PRPH2, RDH5, RHO, RLBP1 - -
02661 - dystrophy, retinal, Bothnia 607475 AR - - RLBP1 eyes -
02662 NFRCD Newfoundland rod-cone dystrophy (NFRCD) 607476 - - - RLBP1 - -
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