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
03367 OCMD dystrophy, macular, occult (OCMD) 613587 AD 40 39 RP1L1 - -
06802 RP88 retinitis pigmentosa, type 88 618826 AR - - RP1L1 - -
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