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
04577 CCMD dystrophy, macular, with central cone involvement (CCMD) 616170 AR - - MFSD8 - -
05258 CLN lipofuscinosis, ceroid, neuronal (CLN) - - 1208 1188 CLCN6, CLN3, CLN5, CLN6, CLN8, DNAJC5, MFSD8, PPT1, TPP1 - -
02997 CLN7 lipofuscinosis, ceroid, neuronal, type 7 (CLN7) 610951 AR 82 81 MFSD8 - -
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