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
02927 CORD10 dystrophy, cone-rod, type 10 (CORD-10) 610283 AR - - SEMA4A - -
02926 RP35 retinitis pigmentosa, type 35 (RP35) 610282 AD;AR - - SEMA4A - -
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